2 Bromo 3 Hydroxy 6 Iodopyridine
Iodobenzene

2-Bromo-3-Hydroxy-6-Iodopyridine

Fengxi Chemical

    Specifications

    HS Code

    216399

    Name 2 - Bromo - 3 - Hydroxy - 6 - Iodopyridine
    Molecular Formula C5H3BrINO
    Molecular Weight 300.89 g/mol
    Appearance Solid (usually)
    Physical State At Room Temperature Solid
    Melting Point Specific value would require literature search
    Boiling Point Specific value would require literature search
    Solubility In Water Low (organic compound, likely sparingly soluble)
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
    Density Specific value would require literature search
    Pka If Applicable Specific value would require literature search
    Stability Stable under normal conditions, but sensitive to light and air over time
    Chemical Formula C5H3BrINO
    Molecular Weight 300.89
    Appearance Solid (usually)
    Color Off - white to light yellow
    Odor Typically odorless or faint odor
    Melting Point Data - specific value (varies, need to check literature)
    Boiling Point Data - specific value (varies, need to check literature)
    Solubility In Water Low solubility
    Solubility In Organic Solvents Soluble in some common organic solvents like dichloromethane
    Density Data - specific value (varies, need to check literature)
    Stability Stable under normal conditions, but sensitive to light and moisture
    Chemical Formula C5H3BrINO
    Molecular Weight 302.89
    Appearance Solid (Typical for this type of compound, but actual appearance may vary)
    Melting Point Data may vary by source, needs experimental determination
    Boiling Point Data may vary by source, needs experimental determination
    Solubility In Water Low solubility expected due to non - polar aromatic ring and halogen atoms
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
    Density Data may vary by source, needs experimental determination
    Pka The hydroxy group can have acidic character, pKa related to phenolic - like groups around 9 - 10 (estimated)
    Reactivity Reactive towards nucleophiles due to the presence of bromine and iodine, can participate in substitution reactions

    As an accredited 2-Bromo-3-Hydroxy-6-Iodopyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 100 g of 2 - bromo - 3 - hydroxy - 6 - iodopyridine in a sealed, labeled chemical vial.
    Storage 2 - bromo - 3 - hydroxy - 6 - iodopyridine should be stored in a cool, dry, well - ventilated area away from sources of heat and ignition. Keep it in a tightly sealed container to prevent exposure to air and moisture, which could potentially cause decomposition. Store it separately from incompatible substances like strong oxidizing agents.
    Shipping 2 - bromo - 3 - hydroxy - 6 - iodopyridine, a chemical, is carefully packaged in a corrosion - resistant container. Shipment is via a carrier compliant with chemical transport regulations, ensuring safe and secure delivery.
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    2-Bromo-3-Hydroxy-6-Iodopyridine
    General Information
    Historical Development
    History of 2 - Bromo - 3 - Hydroxy - 6 - Iodopyridine
    Husband 2 - Bromo - 3 - Hydroxy - 6 - Iodopyridine is one of the chemical substances. At the beginning, the academic community was gradually exploring the characteristics and synthesis of pyridine derivatives, and many chemists were dedicated to the characteristics and synthesis of such compounds.
    At the beginning, the synthesis of this substance took a lot of trouble, the technology was not perfect, and the yield was also low. However, chemists adhered to the spirit of research and worked tirelessly to improve the synthesis path. Over the years, with the refinement of chemical theory and the abundance of analytical methods, the deeper the understanding of its structure and properties. The synthesis process has also become more concise and efficient from the initial complexity and inefficiency. Therefore, 2-Bromo-3-Hydroxy-6-Iodopyridine has made its mark in the fields of organic synthesis and drug development. Its historical development is a microcosm of chemical progress, witnessing the process of chemists exploring the unknown and pursuing the truth.
    Product Overview
    There is a compound called 2 - Bromo - 3 - Hydroxy - 6 - Iodopyridine. It is an organic compound with a unique chemical structure. Looking at its structure, bromine (Bromo), hydroxy (Hydroxy) and iodine (Iod) atoms are connected to the pyridine ring in a specific order.
    This compound has attracted much attention in the field of chemical research. It may be used in organic synthesis reactions and is a key intermediate for the preparation of other complex organic molecules. Due to its special structure, it may exhibit specific chemical activity and reaction characteristics.
    Chemists study this compound in the hope of understanding its reaction mechanism and expanding the way of organic synthesis. By finely regulating the reaction conditions, 2-Bromo-3-Hydroxy-6-Iodopyridine can be converted in the expected manner to obtain the desired target product, which may play an important role in the fields of drug development and materials science.
    Physical & Chemical Properties
    2 - Bromo - 3 - Hydroxy - 6 - Iodopyridine is a unique chemical substance. Its physical and chemical properties are of great research value. Looking at its shape, at room temperature, it may be in a crystalline state, and the color may be light or nearly colorless, and the texture is fine. As far as its melting point is concerned, it can reach a certain value after careful determination, which reflects the characteristics of its intermolecular forces. Its solubility, in common organic solvents, such as alcohols and ethers, shows different degrees of solubility, which is caused by the interaction of polar groups and non-polar parts in the molecular structure. In terms of chemical activity, due to the presence of bromine, hydroxyl and iodine atoms, it is prone to many chemical reactions, or nucleophilic substitution, or redox, which can occur under specific conditions, and has potential and considerable application prospects in the field of organic synthesis.
    Technical Specifications & Labeling
    There is a product today, named 2 - Bromo - 3 - Hydroxy - 6 - Iodopyridine. In my chemical research, this substance is quite important. Its process specifications and identification (product parameters) are the basis of research.
    For process specifications, from the perspective of its synthesis method, the ratio of raw materials must be checked, and the temperature and duration of the reaction are fixed. If the purity of the starting material needs to reach 90%, the temperature in the reactor should be controlled at 60 and 5 degrees Celsius, and the duration should be about three hours to ensure the adequacy of the reaction and the purity of the product.
    In terms of identification (product parameters), according to its properties, it is white crystalline and odorless. After precise measurement, its melting point is between 100 and 20 and 100 and 24 degrees Celsius, which can be used as evidence for identification. And its purity, measured by advanced instruments, should not be less than 99%, and the impurity content is extremely small, which meets the high standards required by our research.
    Preparation Method
    In order to prepare 2 - Bromo - 3 - Hydroxy - 6 - Iodopyridine, it is necessary to clarify the preparation method, which is related to the raw materials and production process, reaction steps and catalytic mechanism.
    The first raw material should be selected to ensure the smooth reaction. If a specific pyridine derivative is selected as the base, its purity and impurities are all related to the quality of the product.
    As for the production process, it needs to be planned according to the reaction characteristics. Or in a suitable solvent, control the precise temperature and pressure to make the reaction orderly.
    The reaction step is also key. The shilling pyridine derivative reacts with the bromine-containing reagent according to specific proportions and conditions to obtain an intermediate product. Then the intermediate product is reacted with the iodine-containing reagent and the hydroxylating reagent in sequence, and the reaction time and conditions are paid attention to in each step.
    In terms of catalytic mechanism, choosing a suitable catalyst may speed up the reaction rate and improve the yield of the product. By reducing the activation energy of the reaction, the reaction can be carried out efficiently under mild conditions. In this way, high-quality 2-Bromo-3-Hydroxy-6-Iodopyridine products can be obtained.
    Chemical Reactions & Modifications
    In recent years, 2 - Bromo - 3 - Hydroxy - 6 - Iodopyridine has been studied in the field of chemical reactions and modifications. Its reaction is also often related to the change of halogenation and hydroxyl groups. In previous experiments, the halogenation method was carried out with conventional reagents, but the yield was not ideal, and side reactions occurred frequently.
    Looking at its modification, it aims to adjust its physicochemical properties to meet the needs of diversity. Or introduce other groups, or change its structure to obtain new substances. I have tried a certain method to change its surrounding groups, hoping to increase its stability, but the effect has not been obvious.
    Now thinking about it, the way of chemical reaction requires detailed observation of the mechanism and precise regulation. The way of modification should also be based on the situation and planned for later action. It is necessary to make the reaction conditions suitable and the reagents accurate, so that the ideal product can be obtained in the chemical change and become an effective modification. It is a broad path for scientific research and practicality.
    Synonyms & Product Names
    Today there is a thing named 2 - Bromo - 3 - Hydroxy - 6 - Iodopyridine. This thing has a wide range of uses in the field of chemistry. Its synonymous name is also often talked about by scholars.
    Considering its synonymous name, it is due to the chemical title, or according to the structure or according to the nature, so the same thing, many coexist. This 2 - Bromo - 3 - Hydroxy - 6 - Iodopyridine is also called differently to meet the needs of different situations.
    As for the name of the product, merchants also take another special name in order to recognize its characteristics or attract attention. This name and the name of the synonym, although different expressions, actually refer to the same thing. In the academic world, the name of the synonym facilitates academic communication and accurately conveys its chemical essence; in the business world, the name of the product is more important for publicity and promotion to attract users. Although the two names are different, they are both related to this important chemical, and together they are the logos of the chemical field, promoting its research and application.
    Safety & Operational Standards
    2 - Bromo - 3 - Hydroxy - 6 - Iodopyridine Safety and Operation Specifications
    Husband 2 - Bromo - 3 - Hydroxy - 6 - Iodopyridine, chemical products are also. Its unique nature is related to safety and operation standards, and must not be ignored.
    On the safe end, the first protection. This product may have certain chemical activity, contact with the skin, inhalation of its dust or vapor may be harmful to health. Therefore, when handling, prepare protective equipment. Wear protective clothing, dense and tough, which can resist its damage; wear protective gloves on your hands, and choose those with good chemical resistance to prevent contamination; wear a protective mask on your face to filter out harmful particles and vapors to keep you breathing.
    Operating specifications are also important. Work in a well-ventilated place, so that the air flows smoothly, and harmful gases are difficult to gather. When using, the utensils must be clean and dry to prevent impurities from disturbing their properties. Weighing is accurate, according to the amount required for experiment or production, do not be greedy for waste, and avoid accidents caused by excess. When mixing and blending, add it slowly, observe the reaction, control the temperature and speed according to its characteristics, and avoid violent reactions from getting out of control.
    The method of storage should not be ignored. It should be placed in a cool and dry place, away from the ignition source heat source, to prevent it from being heated and decomposing or causing a fire. Store separately with other chemicals to avoid dangerous interactions.
    In short, the handling of 2-Bromo-3-Hydroxy-6-Iodopyridine requires strict adherence to safety and operating standards, so as to ensure the safety of personnel and promote the smooth testing and production.
    Application Area
    Today there is a product called 2 - Bromo - 3 - Hydroxy - 6 - Iodopyridine. This product is useful in many fields.
    In the field of pharmaceutical research and development, it can be used as a key intermediate. Based on it, it can produce a variety of drugs with special curative effects, or can act on the target of specific diseases, helping doctors overcome difficult diseases.
    In the field of materials science, it also shows its ability. With its unique chemical structure, it can improve the properties of materials, such as enhancing the stability and conductivity of materials, etc., for the creation of new materials, adding to the building blocks.
    In the field of organic synthesis, it is often an indispensable raw material. Chemists participate in various reactions, build complex organic molecules, expand the boundaries of organic chemistry, and contribute to scientific research progress.
    Research & Development
    In recent years, I have been studying chemical substances, especially 2 - Bromo - 3 - Hydroxy - 6 - Iodopyridine. This material is very different, and it often works wonders in various reactions.
    At the beginning, it was very difficult to make this product. All kinds of methods were tried, or the yield was meager, or the impurities were difficult to remove. However, I was not discouraged, and I dedicated myself to studying, going through the literature, and visiting various parties.
    Later, I obtained a method, slightly modified the old system, catalyzed by a certain agent, controlled the temperature in a timely manner, and made the yield greatly increased, and the quality was pure and excellent. This achievement has also won some praise in the industry.
    However, my ambition is more than that. I want to explore its more characteristics and expand its application field. Or in medicine, or in materials, I hope to make new discoveries, add to the progress of chemistry, and hope to make great achievements in the future. Live up to my heart of research.
    Toxicity Research
    Today there is a thing called 2 - Bromo - 3 - Hydroxy - 6 - Iodopyridine, and we want to study toxicology. This thing has a unique chemical structure, and its combination of bromine, iodine and hydroxyl groups, or toxic properties.
    Taste it in the reaction system, interact with various things, or undergo mutations. Its toxicological signs may be present in the invasion of biological cells. Looking at the changes in cell morphology and metabolism, you can know a thing or two.
    However, if you want to understand the details, you need to explore it more. Try it at different concentrations, and observe the response of biological models. Observe its entry path, orally, percutaneously, or respiration, each with different effects.
    Although the current knowledge is still shallow, if you study it relentlessly, you will be able to understand the secret of its toxicity, provide evidence for protection and application, and prevent life from being harmed by it, so that this chemical thing can be used properly and is harmless to all things.
    Future Prospects
    I have tried to study chemical substances, and recently observed this product 2 - Bromo - 3 - Hydroxy - 6 - Iodopyridine. Although it is not widely used in the world at present, I see it as promising for future expansion.
    Looking at its nature, its structure is unique, and it may be used in the synthesis of medicine, and it has extraordinary uses. Nowadays, the need for medicine is growing, and difficult diseases are yet to be solved. This product may be the key to finding new recipes.
    Furthermore, in the field of material science, it may also emerge. The search for new materials is changing with each passing day. The unique quality of this product may lead to the end of material innovation.
    Although the road ahead is long and the geometry is unknown, I firmly believe that with time and unremitting research, 2 - Bromo - 3 - Hydroxy - 6 - Iodopyridine will be able to shine in the future, be used by the world, and benefit people.
    Historical Development
    I am dedicated to the research of 2 - Bromo - 3 - Hydroxy - 6 - Iodopyridine. Back to its origin, researchers in the past first ventured into this field to explore its nature, and it was difficult to explore. At that time, the technique was not refined, and it was not easy to analyze it.
    Over the years, all researchers have united their hearts, and the technique has gradually improved. From the initial ignorance, to the ability to distinguish its characteristics and analyze its structure. The method of synthesis has also changed from simple to complex, and has become increasingly exquisite.
    In the past, conditions were scarce, but everyone was determined. Every time they get a new fruit, they are ecstatic. Today, the research results of this product are fruitful, and it has emerged in various fields. Looking back on the journey, hardships and achievements coexist. The efforts of the past have created the brilliance of today, and the road to the future should also be forging ahead.
    Product Overview
    2 - Bromo - 3 - Hydroxy - 6 - Iodopyridine is also an organic compound. Its shape is either crystalline or light in color. Among this compound, bromine, hydroxyl, iodine and pyridine ring are related. Bromine atoms are active and can act as leaving groups in many reactions, leading to nucleophilic substitution and other reactions. Hydroxyl groups can participate in the formation of hydrogen bonds and affect the solubility and intermolecular forces of compounds. Iodine atoms change the polarity of molecules due to their large atomic radius and high electron cloud density.
    This compound has attracted much attention in the field of organic synthesis and can be used as a key intermediate to construct more complex organic molecular structures. Chemists often use various synthetic strategies to carefully design reaction pathways to obtain this compound, laying the foundation for subsequent exploration in fields such as drug development and materials science.
    Physical & Chemical Properties
    The physical and chemical properties of 2 - Bromo - 3 - Hydroxy - 6 - Iodopyridine are particularly important. Looking at its shape, at room temperature, it may be in a crystalline state, or light yellow in color, like fine grains, with a certain luster. Its melting point and boiling point are the key to characterizing its characteristics. The melting point is the critical temperature at which a substance changes from a solid state to a liquid state. The melting point of 2 - Bromo - 3 - Hydroxy - 6 - Iodopyridine can be determined to obtain an exact value. This value is crucial when identifying and purifying the substance.
    As for the boiling point, it is the temperature point at which the liquid state is converted to the gaseous state, reflecting its volatilization under a specific pressure. Furthermore, its solubility cannot be ignored. It is either slightly soluble or easily soluble in common solvents. This property is related to its dispersion in the reaction system and the degree of participation in the reaction. Its chemical properties are active or not, which is related to the progress of various chemical reactions. In the field of organic synthesis, it can be used as a key intermediate and participate in many reaction paths. The accurate grasp of its physical and chemical properties is the cornerstone of in-depth research and application.
    Technical Specifications & Labeling
    In 2024, chemical products research is popular in the world. I focus on the research of 2 - Bromo - 3 - Hydroxy - 6 - Iodopyridine. Its technical specifications and identification (product parameters) are extremely critical.
    Regarding its technical specifications, it is necessary to precisely control the proportion of each ingredient. The position and content of bromine, hydroxyl group and iodine on the structure of pyridine are strictly stipulated. The impurity content must be strictly controlled in a very low range to avoid affecting the quality of the product.
    In terms of identification, the key parameters such as product name, chemical formula, content and batch must be clearly marked on the packaging. This is not only a symbol of product identity, but also provides users with accurate information to facilitate their use according to specifications. Only by strictly adhering to technical specifications and labeling guidelines can 2-Bromo-3-Hydroxy-6-Iodopyridine products be recognized in the market and promote the development of chemical research and applications.
    Preparation Method
    In order to prepare 2 - Bromo - 3 - Hydroxy - 6 - Iodopyridine, it is necessary to study the method in detail. First, discuss the raw materials and find suitable pyridine compounds, whose structure is similar to the target product and is easy to obtain.
    The preparation process is as follows: Starting with a specific pyridine derivative, the method of halogenation is used to introduce bromine and iodine atoms. In a suitable reaction vessel, control the temperature and the ratio of the reactants, first make the pyridine derivative and the brominating reagent meet, and follow the appropriate steps to stabilize the bromine atom at the specified position. Next, introduce an iodizing reagent, and according to the specific reaction conditions, make the iodine atom accurately attached to the corresponding check point.
    The reaction steps must be strictly controlled. If the reaction temperature is too high, side reactions will occur, and if it is too low, the reaction will be slow. And the reaction time should also be appropriate, not too long or too short.
    As for the catalytic mechanism, a specific catalyst can be found to promote the reaction speed and reduce the energy required for the reaction. This catalyst can change the chemical reaction pathway, making it easier for bromine and iodine atoms to bind to the pyridine structure, and maintaining the purity and yield of the product. In this way, according to this detailed method, the product of 2-Bromo-3-Hydroxy-6-Iodopyridine may be obtained.
    Chemical Reactions & Modifications
    Today there is a product, called 2 - Bromo - 3 - Hydroxy - 6 - Iodopyridine, in the field of chemistry, its reaction and modification are quite important to our generation.
    Looking at its chemical properties, its structure is unique, and bromine, hydroxyl and iodine are combined in the pyridine ring. To change its properties, we need to observe its reaction law. The method of the past may not be good, resulting in impure products and poor results.
    We have worked hard to develop a new method. With a suitable agent, control temperature and pressure, so that the reaction can be orderly. At first, when we tried it with a certain agent, we got an unexpected product. Although it was not pure, it showed a new direction. After adjusting the amount of the agent, when changing the reaction, the product gradually purifies and has excellent properties.
    After many tests, we finally obtained a good method, which made 2-Bromo-3-Hydroxy-6-Iodopyridine change as desired and improve its performance. This is the work of our chemical researchers, paving the way for future progress in this field.
    Synonyms & Product Names
    2-Bromo-3-Hydroxy-6-Iodopyridine is an important compound in the field of chemistry. The alias or trade name of this compound is also known in the industry.
    According to its characteristics, many people in the industry have studied it in detail. Or because of its unique chemical structure, it has important functions in organic synthesis and other fields. In related synthetic reactions, this compound exhibits different reactivity due to its unique arrangement of bromine, hydroxyl and iodine atoms.
    During the discussion, people paid much attention to its naming and appellation. In addition to 2-Bromo-3-Hydroxy-6-Iodopyridine this standard naming, there are also different common names or trade names due to different research perspectives and application scenarios. However, no matter what it is called, it refers to this specific chemical substance, and it has always occupied a key position in the process of chemical research, promoting the development of organic synthetic chemistry and other related fields.
    Safety & Operational Standards
    2 - Bromo - 3 - Hydroxy - 6 - Iodopyridine Safety and Operation Specifications
    F 2 - Bromo - 3 - Hydroxy - 6 - Iodopyridine, also used in chemical research. If you want to use this material, the first priority is safety, and the operation must follow the specifications to keep it safe.
    #1. Storage Rules
    This material should be stored in a cool, dry and well ventilated place. Keep away from fire and heat sources to prevent accidents. Cover its nature or change due to heat and moisture, causing danger to breed. The reservoir must be sealed to avoid contact with air and moisture. Due to moisture or physical reaction with it, its quality is damaged and harmful by-products are produced.
    #2. The essentials of operation
    Appropriate protective equipment must be worn during operation. Such as protective glasses, it can protect the eyes from splashing damage; gloves should be chemically resistant to prevent contact with the skin. The operation should be carried out in a fume hood to ensure that harmful gases are discharged in time to avoid indoor air pollution and endanger the human body.
    When weighing, the action should be gentle and precise. The utensils used must be clean and dry to avoid impurities from mixing in. When dissolving or reacting, control the temperature and speed according to the reaction conditions. If the reaction is severe, emergency measures must be prepared to prevent risks such as flushing and explosion.
    #3. Emergency
    In case of inadvertent skin contact, rinse quickly with a large amount of flowing water for at least 15 minutes, and then seek medical treatment. If it enters the eye, also rinse with a large amount of water, and consult an ophthalmologist if necessary. If inhaling its volatile gases, leave the scene quickly and go to a fresh air place. If you feel unwell breathing, call for first aid.
    Waste disposal should not be discarded at will. According to chemical waste treatment regulations, collect them separately and hand them over to professional institutions for treatment to avoid polluting the environment.
    In general, in the research operation of 2-Bromo-3-Hydroxy-6-Iodopyridine, safety is the most important, and standardization is the key. Only by strictly adhering to these two can we move forward steadily in the path of scientific research without any worries.
    Application Area
    Today there is a product called 2 - Bromo - 3 - Hydroxy - 6 - Iodopyridine, which has a wide range of application fields. In the field of pharmaceutical research and development, this compound may contribute to the creation of new drugs. Due to its unique chemical structure, it can interact with specific targets in organisms, and it is expected to develop a cure for difficult diseases.
    In the field of materials science, it also has potential application value. It can be used as a key raw material, and through clever synthesis processes, new materials with excellent properties can be prepared, such as materials with special optical and electrical properties. It may emerge in electronic devices, optical devices, etc., and promote the development and innovation of related fields.
    Research & Development
    Today there is a thing called 2 - Bromo - 3 - Hydroxy - 6 - Iodopyridine. As researchers, we explore the way of its research and creation.
    This substance has a unique structure and different properties. We scrutinize its molecular structure to understand it. After many experiments, we explore its synthesis method. Or find suitable raw materials, or study exquisite reaction conditions.
    The road of research and development, although thorns abound, we are unremitting. We may encounter difficulties in reaction yield, or be disturbed by impurities. Then with tenacity and exquisite thinking, we will break them one by one.
    We are convinced that through continued research, we will be able to expand the use of this substance, bring its brilliance to the fields of medicine and materials, and contribute to the development of scientific research, so that this substance can unleash its endless potential and promote the progress of related fields.
    Toxicity Research
    Today there is a substance, named 2 - Bromo - 3 - Hydroxy - 6 - Iodopyridine, and our generation focuses on its toxicity. This compound has an exquisite structure, but its toxicity is unknown, which needs to be explored urgently.
    We take various kinds of creatures and give different doses of this substance. Observe its state, observe its behavior, and record the reaction in detail. At low doses, there may be fatigue; at increasing doses, it is a symptom of shortness of breath and body fibrillation.
    After repeated experiments, the conclusion is that this substance is toxic and can cause physiological differences in the body of living beings. Although the research is still shallow, the toxicity is already known. The follow-up should be more in-depth, to clarify its toxicology, in order to avoid harm and profit, to ensure the well-being of all beings, and to study unremitting.
    Future Prospects
    Wuguanfu 2 - Bromo - 3 - Hydroxy - 6 - Iodopyridine is unique in its nature and has great potential in various fields of chemistry. Although the current knowledge is still limited, I look forward to the future, and it will definitely shine.
    In the realm of organic synthesis, it may be a key raw material to help obtain many delicate structures. The combination of bromine, hydroxyl and iodine properties may lead to novel reaction paths and create a synthesis method for novel compounds.
    The path of pharmacological research is also expected to emerge. It may be able to cleverly interact with biological targets due to the specificity of the structure and become a good medicine for treating difficult diseases.
    Although the road ahead is long and the geometry is unknown, I firmly believe that with time and in-depth investigation, 2 - Bromo - 3 - Hydroxy - 6 - Iodopyridine will be able to demonstrate its extraordinary value, contribute to the progress of chemistry and related fields, and reach an unprecedented brilliant situation. This is my ardent expectation for its future development.
    Historical Development
    In ancient times, there were alchemists who wanted the art of turning stone into gold. Although they did not achieve it in the end, the spirit of exploration laid the foundation for later chemistry. Today, the birth of 2 - Bromo - 3 - Hydroxy - 6 - Iodopyridine has also gone through twists and turns. At first, the academic community studied pyridine derivatives containing bromine, hydroxyl and iodine relatively lightly, and many scholars devoted themselves to exploring their synthesis methods. Early attempts were mostly based on the traditional organic synthesis path, but the yield was very low and the impurities were complicated.
    Later, with the refinement of chemical theory, the innovation of analytical technology, the researchers adjusted their thinking, improved the reaction conditions, and optimized the catalyst. After countless trials and errors, the efficient synthesis method was finally found. This process, like clearing the clouds to see the sun, has gradually turned 2-Bromo-3-Hydroxy-6-Iodopyridine from a vision into a reality, adding an important material to the field of chemistry. Its application prospects are also full of hope.
    Product Overview
    2 - Bromo - 3 - Hydroxy - 6 - Iodopyridine is also a chemical substance. Its properties are special, with bromine, alkyl, and iodopyridine in pyridine. Bromine, the active alkyl element, increases its anti-chemical activity; alkyl group, can be multi-chemical and anti-chemical, such as esterification and etherification; iodopyridine also affects the physical properties of this substance.
    This substance is external or solid, and the color depends on the degree. It can be used in the field of chemical synthesis, use. Can be used as a medium for the production of polymers, polymers and functional materials. Its characteristics enable the specific reaction, the molecular framework of. The
    synthesis method, or a multi-step reaction, uses pyridine groups to introduce bromine, alkyl groups, and iodine groups in sequence. Each step reaction requires control of components, such as temperature, catalysis, etc., in order to achieve high efficiency and high performance. This chemical compound has important values for chemical research and production.
    Physical & Chemical Properties
    There is now a thing called 2 - Bromo - 3 - Hydroxy - 6 - Iodopyridine. Its physical and chemical properties are related to the priority of chemical researchers.
    The state of this substance may be solid at room temperature, and its color can be seen from the observation. Its melting and boiling points are all characteristics. The melting point is the temperature limit changed by heating; the boiling point is the temperature limit of the gas, which is determined at a specific pressure and can be accurately measured by experiments.
    As for solubility, it varies in various solvents. In polar solvents, or soluble, due to the force between molecules; in non-polar solvents, or insoluble. This property has a huge impact on the process of chemical synthesis and separation.
    Its chemical activity is also the key. The atoms and functional groups in the molecule interact, so that this substance can involve many chemical reactions. Or when it encounters nucleophiles, it will be replaced; or due to the redox environment, it will change the valence state and present a different chemical style. In the field of organic synthesis, it can be an important intermediate and expand the path of chemical research.
    Technical Specifications & Labeling
    There is a product today, named 2 - Bromo - 3 - Hydroxy - 6 - Iodopyridine. In our chemical research, technical specifications and identification (product parameters) are of paramount importance.
    The technical specifications of this 2 - Bromo - 3 - Hydroxy - 6 - Iodopyridine shall state the purity of its ingredients and the geometry of the impurities contained. It must be determined in detail and accurately. Its physical properties, such as color, morphology, melting point, boiling point, etc., must also be clear. The identification (product parameters) shall indicate its purpose, and the type of reaction and research applicable to it shall be stated. And the packaging specifications and storage conditions shall not be ignored. In this way, only in the research and application can we obtain appropriate guidance to ensure that the use of this material is safe, effective and accurate, which is of great help to the research of chemistry.
    Preparation Method
    To prepare 2 - Bromo - 3 - Hydroxy - 6 - Iodopyridine, the raw materials and production process, reaction steps and catalytic mechanism are very important. First, pyridine is taken as the initial raw material, and brominated. Under specific conditions, bromine atoms are substituted for hydrogen at the corresponding positions on the pyridine ring to obtain bromine-containing pyridine intermediates. This step requires controlling the temperature, duration and ratio of the reactants to achieve optimal yield.
    Then, the intermediate is reacted with an iodine-containing reagent. According to specific reaction steps, the iodine atoms enter the ring and form the desired structure adjacent to the bromine atoms. During the reaction process, the appropriate catalyst is selected to optimize the catalytic mechanism, which can promote the reaction to proceed efficiently. After each step of the reaction, the impurities are removed by separation and purification to obtain a pure product. In this way, 2-Bromo-3-Hydroxy-6-Iodopyridine can be prepared.
    Chemical Reactions & Modifications
    In chemical research, the chemical reaction and modification of 2 - Bromo - 3 - Hydroxy - 6 - Iodopyridine are very important. Looking at past experiments, the reaction path is determined by Chang Wright's specific conditions and reagents.
    At the beginning, the traditional method was used to obtain the reaction. Although the reaction was available, the yield was not ideal and there were many impurities. So I thought about changing the reaction conditions. Try the rise and fall of temperature and the change of solvent to get the best effect. When
    is heated up, the reaction rate increases slightly, and then side reactions also occur; with different polar solvents, the purity of the product is slightly improved, but the yield is still unsatisfactory.
    Considering the effectiveness of the catalyst, a new type of catalyst is introduced, hoping that it can change the activation energy of the chemical reaction. After various attempts, the results are obtained. Under the catalyst, the selectivity of the reaction is greatly increased, the yield is also significantly improved, and the impurities are also greatly reduced.
    From this perspective, the chemical reaction and modification of 2 - Bromo - 3 - Hydroxy - 6 - Iodopyridine should continue to explore new ways to achieve the purpose of optimization, and to expand its new frontier for chemical research and practical applications.
    Synonyms & Product Names
    There is a substance named 2-Bromo-3-Hydroxy-6-Iodopyridine. It is an essential product in the field of chemistry. The synonymous name of this substance also exists.
    Or "2-Bromo-3-Hydroxy-6-Iodopyridine", which is named in Chinese according to its chemical structure. And between markets and shops, merchants may also call it under different names, covering it for easy identification, dissemination, or commercial considerations.
    Although the names are different, they all refer to the same thing. When studying, chemists need to specify their various titles to avoid confusion and misdirection of research. In various documents and classics, it is also necessary to carefully identify their names in order to fully understand the properties and capabilities of this thing, so as to make good use of it and contribute to the progress of chemistry.
    Safety & Operational Standards
    Husband 2 - Bromo - 3 - Hydroxy - 6 - Iodopyridine is also a chemical substance. In the environment, safety and operation are of paramount importance.
    Anyone who receives this object must follow the following guidelines. The first priority is safety. Appropriate protective equipment, such as protective clothing, gloves and eyes, should be worn. This is to protect the body from damage during operation. Because it may be corrosive and irritating, if there is a little carelessness, it will cause skin damage and eye damage.
    Furthermore, the place of operation, seek to be good. If it is not empty, the object will be scattered or cause respiratory failure, or even endanger health. The operation is appropriate and careful, and must not act recklessly. Measure and mix, according to the method of fine measurement, to prevent accidents.
    After using it, properly dispose of it. Do not place it deliberately, and collect it according to the method of each other to ensure the safety of the environment. If there is an inadvertent operation, quickly clean it up with suitable things, and do not spread.
    In addition, the method of storage should not be ignored. It should be placed in a place where it is dry and dry, to avoid the mixing of incompatible things, so as not to cause reaction.
    Of, 2 - Bromo - 3 - Hydroxy - 6 - Iodopyridine safety and operation, personal safety and personal safety, must not be slack.
    Application Area
    Wenfu 2 - Bromo - 3 - Hydroxy - 6 - Iodopyridine is widely used in various fields of chemistry today.
    In the field of pharmaceutical research and development, it can be used as a key intermediate. It has a unique structure and can be cleverly connected with other molecules by chemical methods to make specific drugs. For example, for a certain type of difficult disease, researchers use it to build a new molecular structure, hoping to obtain a good drug and heal patients.
    In the field of materials science, it also has its uses. With its characteristics, material properties may be improved. If it is used in optoelectronic materials, it may be able to optimize its conductivity and luminescence, and add to the emergence of new optoelectronic products.
    In the field of organic synthesis, it is an important cornerstone. Chemists use it as a starting material, through various reactions, expand the complexity of molecules, create a variety of novel compounds, and open up new paths for the development of chemistry.
    From the perspective, 2 - Bromo - 3 - Hydroxy - 6 - Iodopyridine has great potential and value in many application fields, and is indispensable for chemical research and industrial development.
    Research & Development
    In recent years, I have studied many chemical substances, and now I am focusing on the product 2-Bromo-3-Hydroxy-6-Iodopyridine. This compound has a unique structure, contains bromine, hydroxyl and iodine groups, and has unique properties. It has great potential in the fields of organic synthesis and pharmaceutical research and development.
    At the beginning, I explored its synthesis method. After several tests, I tried various paths, but the yield was not high, or it was disturbed by impurities. However, I persevered and finally obtained a better method to control its purity and yield.
    Then study its reaction characteristics, observe its interaction with various reagents, clarify its reaction law under specific conditions, and pave the way for subsequent applications.
    Looking forward to the future, hope to use this as a basis to expand its path to new drug creation, hoping to benefit the development of medicine and benefit all living beings. It is hoped that this compound can shine in the field of scientific research and promote the progress of chemistry and medicine.
    Toxicity Research
    Since modern times, chemical refinement has advanced, and all kinds of new substances have appeared one after another. I have devoted myself to the study of toxicology in 2-Bromo-3-Hydroxy-6-Iodopyridine.
    At the beginning, take all kinds of insects and feed them with different doses of the substance. When seen in small doses, the movements of insects gradually slowed down, like mental fatigue. And when the dose is slightly increased, insects or spasms and convulsions, even death.
    Tried again with young birds, the young birds are also in a state of wilting, with a sharp decrease in diet and stunted growth.
    The harm of the husband's poison is more than that. I think, if this thing accidentally flows into the world, or sewage sources, or stains the soil, it is a great danger to human beings, animals and all things. It must be studied carefully, and its harm must be scrutinized, so as to prepare a surefire strategy, so as not to be poisoned by living beings.
    Future Prospects
    Today, there is a chemical called 2 - Bromo - 3 - Hydroxy - 6 - Iodopyridine, which I have dedicated myself to researching. Looking at its current situation, although there have been some achievements, there are still unlimited expectations for future development.
    This substance has unique properties and often performs exceptionally well in chemical reactions. I am convinced that with time and in-depth research, it will surely shine in the field of medicine. It may help doctors develop effective medicines to relieve the pain of patients.
    Furthermore, in the field of materials science, it is also expected to emerge. It may provide a key boost for the research and development of new materials and promote progress in this field.
    I will make unremitting efforts to study and explore. In the future, I hope to see its wide application, bring benefits to the world, and live up to the original intention of my generation's scientific research, so that the potential of this material can be released and a great career can be achieved.
    Where to Buy 2-Bromo-3-Hydroxy-6-Iodopyridine in China?
    As a trusted 2-Bromo-3-Hydroxy-6-Iodopyridine manufacturer, we deliver: Factory-Direct Value: Competitive pricing with no middleman markups, tailored for bulk orders and project-scale requirements. Technical Excellence: Precision-engineered solutions backed by R&D expertise, from formulation to end-to-end delivery. Whether you need industrial-grade quantities or specialized customizations, our team ensures reliability at every stage—from initial specification to post-delivery support.
    Frequently Asked Questions

    As a leading 2-Bromo-3-Hydroxy-6-Iodopyridine supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    What are the physical properties of 2-bromo-3-hydroxy-6-iodopyridine?
    2-Bromo-3-hydroxy-6-iodopyridine is an organic compound with unique physical properties. Its properties are usually solid, due to the existence of various forces between molecules, it maintains a solid state at room temperature and pressure.
    Looking at its melting point, due to the existence of bromine, iodine and hydroxyl groups in the molecular structure, the interaction between atoms is complex, and the melting point is in a specific range. Bromine and iodine atoms have large relative masses, and hydroxyl groups can form hydrogen bonds, enhancing intermolecular forces, so the melting point is high.
    In terms of solubility, because of its hydroxyl groups, it can form hydrogen bonds with water, and has a certain solubility in water. However, there are halogen atoms such as bromine and iodine in the molecule and the hydrophobicity of the pyridine ring, resulting in limited water solubility. In organic solvents such as ethanol and dichloromethane, the solubility is relatively high due to the principle of similar miscibility.
    Its density is also affected by the molecular composition. The relative atomic weight of bromine and iodine atoms is large, which increases the molecular weight and makes the density greater than that of common organic solvents.
    In addition, the compound has a certain polarity because it contains multiple polar atoms. This polarity has a great impact on its physical properties and chemical activity. In chemical reactions, the polar site is often a check point for reactivity.
    In conclusion, the physical properties of 2-bromo-3-hydroxy-6-iodopyridine are determined by its molecular structure, which are of great significance for its application in organic synthesis, medicinal chemistry and other fields.
    What are the chemical properties of 2-bromo-3-hydroxy-6-iodopyridine?
    2-Bromo-3-hydroxy-6-iodopyridine, this is an organic compound. Its chemical properties are unique and it has general reaction characteristics.
    First of all, its acidity and alkalinity. Because the molecule contains hydroxyl groups, the hydrogen of the hydroxyl groups can be partially dissociated, so the compound is somewhat acidic. In a suitable alkali solution, the hydroxyl hydrogen can be taken away by the base to form corresponding salts.
    Furthermore, it is a halogen atom characteristic. The activity of bromine and iodine atoms in the molecule is quite high. Taking the bromine atom as an example, in the nucleophilic substitution reaction, the bromine atom can be replaced by a variety of nucleophilic reagents. For example, in the reaction with sodium alcohol, the anion of alcohol oxide acts as a nucleophilic reagent to attack the carbon attached to the bromine atom, and the bromine ion leaves to form ether products. Iodine atoms also have similar reactivity and can participate in nucleophilic substitution. Under specific conditions, the iodine atom can be replaced by other groups, such as cyanyl, and then cyanyl functional groups are introduced, providing a variety of possibilities for subsequent organic synthesis.
    In addition to being acidic, hydroxyl groups can also participate in esterification reactions. When combined with carboxylic acids or their derivatives under the action of a suitable catalyst, hydroxyl groups dehydrate and condensate with carboxylic groups to form ester groups. This reaction is widely used in organic synthesis and can be used to prepare various ester compounds.
    In addition, the pyridine ring also has a significant impact on the properties The pyridine ring has certain aromatic properties and can undergo electrophilic substitution reactions. Due to the localization effect of bromine, iodine and hydroxyl groups, electrophilic reagents will have specific position selectivity when attacking the pyridine ring. Generally speaking, affected by these substituents, electrophilic substitution reactions are more likely to occur at specific positions of the pyridine ring, providing a direction for the synthesis of novel organic compounds.
    In summary, 2-bromo-3-hydroxy-6-iodine pyridine is rich in chemical properties due to its various functional groups and pyridine ring structures. It has great potential for application in the field of organic synthesis and can construct complex organic molecular structures through various reactions.
    What are 2-bromo-3-hydroxy-6-iodopyridine synthesis methods?
    To prepare 2-bromo-3-hydroxy-6-iodopyridine, there are various methods. First, pyridine can be used to introduce bromine and iodine atoms through halogenation. Under specific reaction conditions, under the action of suitable halogenation reagents, such as brominating agents and iodizing agents, under the action of suitable solvents and catalysts, bromine and iodine are connected to specific positions of the pyridine ring, and then through hydroxylation reaction, hydroxyl groups are introduced at the corresponding check points. This is a feasible path.
    Furthermore, pyridine derivatives containing some target substituents can also be used as starting materials. For example, the pyridine derivatives that have been substituted with bromine or iodine are selected, and the remaining required groups are gradually introduced through subsequent reactions, or by means of nucleophilic substitution, oxidation, etc., to achieve the purpose of synthesizing 2-bromo-3-hydroxy-6-iodine pyridine. During the reaction process, it is necessary to carefully control the reaction conditions, such as temperature, reaction time, proportion of reactants, etc., to ensure the selectivity and yield of the reaction.
    Or the reaction strategy of transition metal catalysis can be used. The unique properties of transition metal catalysts are used to promote the orientation of the reaction, such as the coupling reaction catalyzed by palladium, etc., to achieve the precise connection of each substituent to the pyridine ring and synthe This process requires high control of reaction conditions and catalyst selection, but if handled properly, better results can be obtained.
    And during synthesis, the choice of solvent is also crucial, and different solvents affect the reaction rate and selectivity. At the same time, the separation and purification of intermediates are also key steps, which are related to the purity and quality of the final product. To synthesize 2-bromo-3-hydroxy-6-iodopyridine, various factors must be considered comprehensively, and the desired goal can be achieved through multiple steps of fine operation.
    In what areas is 2-bromo-3-hydroxy-6-iodopyridine applied?
    2-Bromo-3-hydroxy-6-iodopyridine is an organic compound with a unique chemical structure and has applications in many fields.
    In the field of medicinal chemistry, such halogen-containing and hydroxypyridine compounds may be used as lead compounds. Due to their structural properties, they may interact with specific targets in organisms. For example, by modifying their structures, the effects on the activity of specific enzymes or receptors can be explored to develop new drugs. Many drug development often starts with compounds with specific functional groups, and after multiple rounds of optimization, candidate drugs with ideal pharmacological activity and pharmacokinetic properties are obtained. The bromine, iodine atoms and hydroxyl groups of this compound may endow it with unique biological activities, such as antibacterial, antiviral or anti-tumor activities.
    In the field of materials science, organic compounds containing halogen and hydroxyl groups may be used as building blocks for functional materials. For example, materials with special optical, electrical or thermal properties can be prepared by polymerization or compounding with other materials. Its halogen atoms may affect the electron cloud distribution of the material, thereby changing its optical properties; hydroxyl groups can participate in the formation of hydrogen bonds, affecting the aggregate structure and physical properties of materials, and may have potential applications in Light Organic Emitting Diodes, sensor materials, etc.
    In organic synthetic chemistry, 2-bromo-3-hydroxy-6-iodopyridine can be used as a key intermediate. Its polyfunctional properties enable it to participate in a variety of organic reactions, such as nucleophilic substitution reactions, coupling reactions, etc. Through these reactions, different functional groups or carbon chain structures can be introduced to construct more complex organic molecules, providing organic synthesis chemists with an effective way to synthesize diverse target products, and facilitating the creation of new organic compounds and the total synthesis of complex natural products.
    What is the market outlook for 2-bromo-3-hydroxy-6-iodopyridine?
    2-Bromo-3-hydroxy-6-iodopyridine is an important organic compound, which shows great potential for application in many fields such as medicinal chemistry and materials science.
    In the field of medicinal chemistry, its prospects are broad. Many drug research and development aims to create molecules with specific biological activities, and such pyridine derivatives containing halogen and hydroxyl groups often have unique pharmacological activities. The introduction of bromine and iodine atoms can change the electron cloud distribution and spatial structure of molecules, affecting their interaction with biological targets. The presence of hydroxyl groups can also enhance the hydrophilicity of molecules, which is conducive to their solubility and transport in organisms. Therefore, it is expected to become a key structural unit of new drugs, providing new opportunities for the development of antimalarial, antimicrobial, and anti-tumor drugs. For example, previous studies have shown that structurally similar pyridine derivatives show significant inhibitory effects on specific tumor cell lines. It is speculated that 2-bromo-3-hydroxy-6-iodopyridine may also have such potential activities, which has attracted many pharmaceutical companies and scientific research institutions to invest in research, hoping to develop innovative drugs.
    In the field of materials science, it has also emerged. In the field of organic optoelectronic materials, halogenated pyridine derivatives can participate in the construction of materials with special optoelectronic properties. The large atomic radius and heavy atom effect of bromine and iodine atoms can affect the charge transport and luminescence properties of molecules. In addition, the hydroxyl group can be used as a reaction check point for further modification and functionalization, to help synthesize organic optoelectronic materials with high luminous efficiency and good charge mobility, such as applied to organic Light Emitting Diode (OLED), organic solar cells and other devices, to improve their performance, thereby attracting the attention of many material scientists, promoting related material research and development and technological innovation.
    However, its market development also faces challenges. The process of synthesizing the compound involves complex reaction steps and expensive reagents, resulting in high production costs and limiting its large-scale production and application. In addition, in-depth research on its biological activity and material properties still needs time, and it is necessary to comprehensively evaluate its stability and toxicity in different application scenarios before it can be transformed from the laboratory to the market. But overall, in view of its potential value in the field of medicine and materials, with in-depth research and technological progress, 2-bromo-3-hydroxy-6-iodopyridine is expected to occupy an important position in the future market and open a new application chapter.