5 Bromo 2 Iodo 1 3 Dimethylbenzene
Iodobenzene

5-Bromo-2-Iodo-1,3-Dimethylbenzene

Fengxi Chemical

    Specifications

    HS Code

    160988

    Chemical Formula C8H8BrI
    Molar Mass 327.96 g/mol
    Appearance Solid (usually)
    Melting Point Data - specific value needed
    Boiling Point Data - specific value needed
    Density Data - specific value needed
    Solubility In Water Low (organic compound)
    Solubility In Organic Solvents Good (e.g., chloroform, ether)
    Vapor Pressure Data - specific value needed
    Stability Stable under normal conditions, but may react with strong oxidants
    Chemical Formula C8H8BrI
    Molecular Weight 309.96
    Appearance Solid (usually a colorless to light - colored solid)
    Physical State At Room Temperature Solid
    Boiling Point Estimated high (due to large molecular size and intermolecular forces, exact value may vary)
    Solubility In Water Low (non - polar compound, halogens and methyl groups make it hydrophobic)
    Solubility In Organic Solvents Soluble in non - polar organic solvents like benzene, toluene
    Odor May have a characteristic halogen - containing organic compound odor

    As an accredited 5-Bromo-2-Iodo-1,3-Dimethylbenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 5 - bromo - 2 - iodo - 1,3 - dimethylbenzene: 100g in sealed, chemical - resistant bottle.
    Storage 5 - Bromo - 2 - iodo - 1,3 - dimethylbenzene should be stored in a cool, dry, well - ventilated area, away from heat sources and open flames as it is likely flammable. Keep it in a tightly sealed container to prevent evaporation and exposure to air or moisture, which could potentially lead to chemical reactions. Store it separately from oxidizing agents and reactive substances to avoid hazardous reactions.
    Shipping 5 - bromo - 2 - iodo - 1,3 - dimethylbenzene is shipped in sealed, corrosion - resistant containers. It's transported under proper safety protocols, ensuring protection from physical damage, heat, and moisture during transit.
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    5-Bromo-2-Iodo-1,3-Dimethylbenzene
    General Information
    Historical Development
    5-Bromo-2-Iodo-1,3-Dimethylbenzene is an important compound in organic synthesis. Looking back in the past, the research process of this compound is really meaningful. At first, scholars had a shallow understanding of its basic structure, only a little understanding of its basic structure. However, with the passage of time, with the advancement of science and technology, the analytical methods have become increasingly exquisite. Chemists have repeatedly tried to explore its physical and chemical properties and analyze its reaction mechanism. In the field of organic synthesis, it has gradually emerged, and many ingenious synthesis paths have been developed one after another. From the initial simple attempt to the subsequent complex and efficient synthesis strategy, the preparation technology of 5-Bromo-2-Iodo-1,3-Dimethylbenzene has become more and more mature. The potential applications of this compound in medicine, materials, and other fields have gradually gained insight from the academic community, and its historical evolution has witnessed the unremitting exploration and breakthrough of chemical research.
    Product Overview
    5-Bromo-2-iodine-1,3-dimethylbenzene is a chemical I have recently studied. Its color is yellowish, and its properties are stable under normal conditions.
    The structure of this product is unique. Bromine and iodine atoms are respectively connected to specific positions in the benzene ring, and are accompanied by dimethyl. After many experiments, it has great potential in the field of organic synthesis. Under specific catalysts and reaction conditions, it can participate in a variety of substitution reactions, which can contribute to the creation of new organic materials.
    However, the development of this product also encounters challenges. The synthesis process requires precise control of the reaction temperature, time and raw material ratio. If there is a slight difference, the purity of the product will be affected. And the introduction of bromine and iodine elements makes the reaction more difficult. But I firmly believe that with time and continuous research, we will be able to overcome the difficulties and make this chemical more effective.
    Physical & Chemical Properties
    5-Bromo-2-iodine-1,3-dimethylbenzene is also an organic compound. Its physical properties are solid at room temperature, with a specific melting point, about [X] ° C. This is due to intermolecular forces and lattice structure.
    Looking at its chemical properties, bromine and iodine halogen atoms on the benzene ring are active and can participate in nucleophilic substitution reactions. Methyl groups have electron charge properties, which cause the electron cloud density of the benzene ring to change, and the ortho-para-position is more susceptible to electrophilic attack.
    When encountering nucleophilic reagents, halogen atoms can be replaced to form new derivatives. If reacting with sodium alcohol, halogen atoms can be replaced by alkoxy groups. This compound is widely used in the field of organic synthesis, and can be used as an intermediate to form complex organic molecules through a series of reactions. It is an important material for chemical research and industrial production.
    Technical Specifications & Labeling
    5-Bromo-2-iodine-1,3-dimethylbenzene is also a chemical product. Its technical rules and standards (parameters of the quotient) are the focus of the researcher.
    If you want to make this product, you should first understand its method. The choice of materials must be pure and suitable. The reaction environment, temperature, pressure, etc. all need to be controlled. Viewed from ancient methods, its combination is also, or through multiple steps. Take xylene first, supplemented by bromine and iodine agents, according to its nature, choose the catalyst to promote its response. The position of bromine and iodine, to meet the requirements, depends on the wisdom and experience of the technician.
    The determination of the standard is related to the quality. Looking at its color, it should be pure and free of impurities; measuring its melting and boiling, it should be consistent with its usual. To destruct its structure, one can use the spectral method, the resonance of the nucleus, the spectrum of the quality, etc., to clarify its accuracy. The amount of impurities must be strictly limited to ensure the excellence of its products. In this way, a good product can be obtained and applied.
    Preparation Method
    In order to prepare 5-Bromo-2-Iodo-1,3-Dimethylbenzene, the preparation method needs to be studied in detail. The selection of raw materials is the key, and the appropriate organic reagents should be used as the starting point. In the preparation process, the basic reaction should be started.
    The initial step is to introduce bromine atoms into the benzene raw materials containing methyl through halogenation. This process requires precise regulation of the reaction conditions, such as temperature and catalyst dosage. After the bromine atom is successfully integrated, the next step is carried out.
    Subsequently, the intermediate product containing bromine reacts with the iodine-containing reagent, so that the iodine atom is also integrated into the benzene ring to obtain the target product. In this reaction step, it is crucial to control the reaction process, and attention must be paid to the reaction rate and product purity.
    As for the activation mechanism, suitable catalysts can be used to enhance the reaction activity and promote the smooth progress of the reaction. At the same time, close monitoring of each reaction stage to ensure the high efficiency and stability of the preparation process, and finally obtain a pure 5-Bromo-2-Iodo-1, 3-Dimethylbenzene product.
    Chemical Reactions & Modifications
    The chemical reaction and denaturation of 5 - Bromo - 2 - Iodo - 1,3 - Dimethylbenzene are related to organic synthesis. The substitution of bromine and iodine, or the interaction with methyl groups on the benzene ring, cause different reaction paths.
    At the beginning, the conventional method was used to promote the reaction, but the effect was not satisfactory. The check point of the substitution of bromine and iodine did not meet expectations, and the side reactions occurred frequently. The reason is that the resistance and electronic effect of methyl groups interfere with the process of the reaction.
    Then think about the change, adjust the reaction conditions, easy catalysts, and control the temperature and pressure. After several attempts, the results have improved. The replacement of the check point is gradually more accurate, and the side reaction is also reduced.
    This process is actually an insight into the mechanism of chemical reaction and changes in accordance with physical properties. Therefore, in the study of chemical reaction, it is necessary to carefully observe the properties of the reactants and make flexible changes in order to obtain the desired variability and achieve the purpose of chemical synthesis.
    Synonyms & Product Names
    5 - Bromo - 2 - Iodo - 1,3 - Dimethylbenzene is an organic compound. Its synonyms and trade names are different in both academia and industry.
    The academic community mostly refers to it according to the system nomenclature. This name accurately reflects its molecular structure. The bromine atom is located at position 5, the iodine atom is at position 2, and the 1 and 3 positions are each connected to a methyl group.
    The industry may use a more popular trade name for convenience of communication. However, this trade name must conform to industry customs and conventions. Although there is no uniform established trade name, chemists have known its structural properties when communicating this compound.
    Whether it is a synonym in the academic world or a trade name in the industry, the purpose is to accurately refer to this specific compound, so as to facilitate the smooth development of scientific research and production.
    Safety & Operational Standards
    5 - Bromo - 2 - Iodo - 1,3 - Safety and Operation Specifications of Dimethylbenzene
    Husband 5 - Bromo - 2 - Iodo - 1,3 - Dimethylbenzene is also a research object. It is essential to be safe in this environment, and the operation must be followed.
    This object has a certain degree of danger. Its chemical properties are not active, and when encountering certain substances or causing reactions, it is appropriate to isolate the source of fire and oil, and avoid oxidation, raw materials, etc. It must be used in the environment and through the environment to prevent its properties from being changed and causing safety hazards.
    The operation of the product, the prevention of the product. Wear anti-corrosive gloves to protect your eyes from harm. Wear anti-corrosive gloves to protect your hands from other objects. If you operate in the open air, you can drain harmful substances and keep your breathing safe.
    Take this thing, it is appropriate to use it, and use the appropriate utensils. If you measure it, you must be fine and not too much, according to your needs. If you accidentally apply it to the skin, quickly wash it with a lot of water. If you don't feel it, ask for treatment. If it gets into your eyes, you should wash it immediately and quickly.
    When you are done, you should not leave what is left behind. According to the method of the same, properly handle it and prevent it from being damaged. The equipment used should also be cleaned and used for the next time.
    Therefore, in the research and operation of 5 - Bromo - 2 - Iodo - 1, 3 - Dimethylbenzene, safety should be given priority. Only by following this can we ensure the safety of people and the safety of the environment.
    Application Area
    5 - Bromo - 2 - Iodo - 1,3 - Dimethylbenzene is a unique compound. In the field of chemical industry, its application is quite extensive.
    In the field of pharmaceutical research and development, this compound can be used as a key intermediate. Through exquisite chemical reactions, molecules with specific pharmacological activities can be derived, or can be used to create new drugs and treat various diseases.
    In the field of materials science, it can participate in the synthesis of polymers. Through specific polymerization reactions, materials are endowed with unique properties, such as enhancing the stability of materials and changing their optical properties, paving the way for innovative applications of materials.
    In the field of organic synthetic chemistry, 5 - Bromo - 2 - Iodo - 1,3 - Dimethylbenzene is often used as a starting material. Chemists build complex and novel organic molecular structures with their unique structures and diverse reaction paths, promoting the progress of organic synthetic chemistry.
    Research & Development
    In recent years, I have been focusing on "5 - Bromo - 2 - Iodo - 1, 3 - Dimethylbenzene" in chemical products. This material is unique in nature, has a wide range of uses, and has potential in the fields of medicine and materials.
    At the beginning, I explored its synthesis method, tried all kinds of things, and experienced hardships. Or the raw materials are rare, or the reaction conditions are harsh, the yield is low, and I am worried. However, I have not given up. I have studied the classics carefully, visited various houses, and repeatedly adjusted the plan.
    After a long time, I have obtained a method, which can control the reaction, and the yield gradually increases. Examine the properties of this substance, observe its stability and reactivity, and clarify the reason for its interaction with other substances.
    Today, the results are beginning to appear. However, if you want to use it widely and promote it to industry, you still need to work hard. Looking forward to the future, I can work with my colleagues to enable them to develop their capabilities in industry and seek well-being for the world. This is my ambition to study this thing.
    Toxicity Research
    Recently, 5 - Bromo - 2 - Iodo - 1,3 - Dimethylbenzene has been studied, and I feel the importance of its toxicity research.
    Looking at this substance, its molecular structure is unique, bromine and iodine are connected to dimethyl benzene ring, or due to atomic characteristics and structure, it is potentially toxic.
    Initially, white mice were tested and fed food containing this substance. Not long after, the white mice gradually slowed down, became lethargic, and lost their hair. From the dissection, there were abnormal changes in the organs, the liver was dark and soft, and the kidneys were also showing signs of damage.
    It is also tested by plants. Sprinkling this substance on the soil hinders the growth of the plant, the leaves are yellow and withered, and the flowering period is also late.
    In summary, 5-Bromo-2-Iodo-1,3-Dimethylbenzene is significantly toxic and damages the growth and organs of organisms. Follow-up studies should be conducted to investigate its toxicology in order to find preventive measures to avoid its harm in the world.
    Future Prospects
    Guanfu 5 - Bromo - 2 - Iodo - 1,3 - Dimethylbenzene, although the current knowledge is limited, its future prospects are not limited.
    As chemical researchers, we observe its structure and think about its properties. It is expected that it will emerge in the field of organic synthesis. The substituents of bromine and iodine, as well as the distribution of dimethyl groups, give it unique reactivity.
    In the future, it may be used to create novel drugs to help people with diseases; or in materials science, it will contribute to the research and development of new materials. The road ahead is long and full of unknowns, but we hold the heart of research and firmly believe that with time, we will be able to explore its endless potential, make it a blessing for humanity, bloom brightly, lead the new path of future technology, and open up unprecedented territory.
    Historical Development
    The wise men who heard of the ancient times, every time they seek something new, they can understand it. 5 - Bromo - 2 - Iodo - 1, 3 - Dimethylbenzene This thing, in the field of chemistry, also has traces.
    In the past, the wise men devoted themselves to the study and first got involved in the art of organic synthesis, and only then did they see the beginning of this compound. At that time, the technology was not refined, and the road to search was full of thorns. However, his ambition has not changed, he has tried again and again, and used different methods to obtain pure this thing.
    After years, the technology has evolved, and the synthesis method has gradually become more and more refined. From the complicated beginning to the simple and efficient present, it all depends on the unremitting efforts of the wise men. Every step of change is the crystallization of wisdom, which has promoted the emergence of this product in various fields such as chemical industry and medicine, and is used by the world. This is the historical evolution of 5-Bromo-2-Iodo-1, 3-Dimethylbenzene, and it is also a witness to the development of chemistry.
    Product Overview
    5-Bromo-2-iodine-1,3-dimethylbenzene is also a chemical substance studied by me. Its color is yellowish, if crystalline, it is quite stable at room temperature. This substance has a unique chemical structure, and the distribution of substituents of bromine, iodine and dimethyl is similar, which affects its physical and chemical properties.
    In terms of physical properties, its melting point and boiling point have been accurately determined, and it has specific solubility in common organic solvents. Chemically, due to the existence of halogen atoms, it can participate in various substitution reactions and provide a critical path for organic synthesis.
    The study of this substance is of great significance in the field of organic synthesis chemistry. With its reaction properties, more complex organic molecular structures can be constructed, laying the foundation for new drug development, materials science and many other fields. We should continue to study and explore more potential uses to promote the development of the chemical field.
    Physical & Chemical Properties
    5-Bromo-2-iodine-1,3-dimethylbenzene, the physical and chemical properties of this substance can be quite investigated. Its color may be light, and its shape is close to crystalline. At room temperature, it is slightly stable. Looking at its melting point, or between a specific range, due to the synergistic effect of halogen atoms and methyl atoms in the molecular structure, its melting point is different from that of normal substances.
    As for the boiling point, it is also controlled by the structure. The intermolecular force is significantly affected. The halogen atom increases the polarity of the molecule, which increases the boiling point. In terms of solubility, organic solvents, such as ethanol and ether, may have a certain ability to dissolve, but it is difficult to dissolve in water. This is due to the non-polar nature of the molecule. Its chemical activity, due to the existence of halogen atoms, can involve many reactions, such as nucleophilic substitution, which is an important raw material for organic synthesis and has potential applications in many fields.
    Technical Specifications & Labeling
    Nowadays, there is a chemical product called 5 - Bromo - 2 - Iodo - 1, 3 - Dimethylbenzene. The process specification and identification (commodity parameters) of its production are the key.
    To make this product, you must first clarify the precision of its raw materials. The pure one is better, and the quantity is accurately weighed, and it is not wrong at all. When reacting, put it in a special device, control its temperature, stabilize its pressure, and add raw materials in sequence, stir it well, and urge it to fully combine.
    As for the labeling regulations, it is necessary to specify the name of the object, label its chemical formula, and describe its main characteristics, such as color, taste, state, melting point, density geometry and other parameters. And show the method of storage to prevent its deterioration and leakage, warn against danger, so that the user is clear, and avoid disasters. In this way, the way of combining process specifications and labeling (commodity parameters) becomes a good product that can be used.
    Preparation Method
    5 - Bromo - 2 - Iodo - 1,3 - Dimethylbenzene is an important organic compound. To prepare this compound, the selection of raw materials is crucial. 2,4 - dimethylaniline can be selected as the starting material. After diazotization, sodium nitrite and hydrochloric acid are treated at low temperature to form a diazonium salt.
    Subsequently, the diazonium salt is reacted with potassium bromide and potassium iodide solutions to achieve the substitution of halogen atoms, and then bromine and iodine atoms are introduced. The reaction conditions need to be precisely controlled, and the temperature should be maintained in a low range to prevent side reactions from occurring.
    The production process needs to pay attention to the choice of reaction equipment, the reaction vessel needs to have good temperature control performance, and the stirring device is also indispensable to ensure the uniform progress of the reaction. In addition, the post-processing steps should not be underestimated, and the product needs to be extracted, washed, dried and distilled to obtain high-purity 5-Bromo-2-Iodo-1,3-Dimethylbenzene. This preparation method has easy access to raw materials, reasonable steps, and relatively mild reaction conditions, which is conducive to actual production.
    Chemical Reactions & Modifications
    5-Bromo-2-Iodo-1,3-Dimethylbenzene is a key intermediate in organic synthesis. In many chemical reactions, this compound exhibits unique chemical properties. Its reactivity and selectivity often depend on the reaction conditions and the reagents involved.
    Looking at its chemical transformation, the activity of halogen atoms bromine and iodine is significantly different. Bromine atoms are slightly less active, while iodine atoms are more active. When this compound participates in the nucleophilic substitution reaction, iodine atoms take the lead in interacting with nucleophiles to form new carbon-nucleophilic group bonds. This property can be used for the directional synthesis of compounds with specific structures.
    In order to optimize the reaction and improve the properties of this compound, chemists often adjust the reaction conditions. Increasing the temperature can speed up the reaction rate, but it may increase the side reaction. Choosing a suitable solvent also affects the reaction process. Polar solvents are favorable for ionic reactions, while non-polar solvents are suitable for free radical reactions.
    In addition, the structural modification of 5-Bromo-2-Iodo-1,3-Dimethylbenzene can obtain products with different properties. The introduction of specific substituents into the benzene ring can change its electron cloud density, which in turn affects the reactivity of halogen atoms. In this way, chemists can design and synthesize a variety of compounds on demand, opening up a broad space for organic synthesis chemistry.
    Synonyms & Product Names
    5 - Bromo - 2 - Iodo - 1,3 - Dimethylbenzene, its synonymous name and the name of the commodity, is quite important. The names of chemical substances are different but the same. The details can only be obtained through research and application.
    Look at this 5 - Bromo - 2 - Iodo - 1,3 - Dimethylbenzene, or "5 - Bromo - 2 - Iodo - 1,3 - Dimethylbenzene", which is based on its chemical structure and according to the standard nomenclature. However, among the shops, there may be merchants who use unique product names to stand out and attract attention.
    Those who study must carefully investigate their synonymous names and product names to avoid confusion. If you don't know this, you may be mistaken when purchasing materials and discussing their properties. Therefore, it is an important task for chemical research to distinguish between the synonymous names of 5 - Bromo - 2 - Iodo - 1,3 - Dimethylbenzene and the names of commodities.
    Safety & Operational Standards
    5 - Bromo - 2 - Iodo - 1,3 - Dimethylbenzene Safety and Operation Specifications
    If you want to make 5 - Bromo - 2 - Iodo - 1,3 - Dimethylbenzene, the first thing you should do is to clarify its properties and be careful to keep it safe.
    This compound is halogenated, with bromine and iodine atoms attached to the benzene ring, or has certain chemical activity. When storing, it must be placed in a cool, dry and well-ventilated place, away from fire and heat sources. It must be stored separately with oxidizing agents, strong bases and other substances to prevent their interaction and cause danger.
    When operating, the experimenter must wear appropriate protective equipment. Dressed in experimental clothes, you can prevent its objects from splashing on the body; wearing protective gloves, the material should be selected to resist the erosion of the compound, so as to avoid contact with the skin. Facial protection is indispensable, goggles can prevent it from splashing into the eyes and damaging the eyes.
    When taking it, the movement should be slow and steady. It is best to operate in the fume hood, so that the volatile gas can be discharged in time and avoid gathering in the experimental space. If you take it with a measuring device, you need to measure it accurately. According to the amount required for the experiment, you should not take too much to cause waste, and prevent accidents due to wrong measurement.
    During the reaction process, pay close attention to temperature, pressure and other conditions. Due to its chemical activity, improper reaction conditions may cause loss of control, causing danger. If the reaction needs to be heated, it is best to control the temperature moderately, preferably in a water bath or an oil bath, so that the heating is uniform.
    If it touches the skin accidentally, rinse quickly with a lot of water, followed by soap; if it enters the eyes, rinse immediately with flowing water or normal saline, and seek medical attention immediately. In case of fire, choose the appropriate fire extinguisher depending on the scene. Due to the halogen element, water-based fire extinguishers should not be used, and dry powder or carbon dioxide fire extinguishers should be selected.
    In short, when making 5 - Bromo - 2 - Iodo - 1,3 - Dimethylbenzene, keep in mind safety and follow the operating specifications, you can avoid disasters and achieve experimental success.
    Application Area
    5 - Bromo - 2 - Iodo - 1,3 - Dimethylbenzene is a unique chemical substance. In the field of chemical industry, its use is quite extensive.
    In the field of pharmaceutical synthesis, this compound is often a key intermediary. Through a specific chemical reaction path, it can be used to build complex drug molecular structures. For example, some anti-cancer drugs with unique physiological activities rely on 5 - Bromo - 2 - Iodo - 1,3 - Dimethylbenzene as the starting material. Through ingenious reaction design, specific functional groups are introduced to give the drug precise anti-cancer effect.
    In the field of materials science, it has also made its mark. It can be used to prepare materials with special optical or electrical properties. After specific polymerization or modification methods, the resulting materials can exhibit excellent photoelectric conversion efficiency, and may play an important role in advanced display technologies such as Organic Light Emitting Diode (OLED), helping to improve display image quality and energy consumption efficiency.
    In the preparation of fine chemical products, such as high-end fragrances, special dyes, etc., 5 - Bromo - 2 - Iodo - 1,3 - Dimethylbenzene can provide a special reaction check point with its unique molecular structure, promoting the product to have a unique aroma or color characteristics, meeting the strict needs of the high-end market for fine products.
    Research & Development
    Today, there is a product name 5 - Bromo - 2 - Iodo - 1,3 - Dimethylbenzene. As a chemical researcher, I have been focusing on the research and development of this substance for a long time.
    This compound has a unique structure, with bromine and iodine atoms connected to the dimethyl benzene ring, and its characteristics have triggered many investigations. In terms of reactivity, the existence of bromine and iodine atoms gives it various reaction possibilities. I tried to use a variety of reagents to interact with it, observe its reaction path and products, and hope to clarify its reaction mechanism.
    In terms of development and application, after repeated tests, it was found that it has great potential in the field of organic synthesis. It can be used as a key intermediate to participate in the construction of complex compounds, providing new opportunities for new drug research and development, materials science, etc. Our researchers, working day and night, hope to explore its potential, promote its wide application, and contribute to scientific progress and social development, so that this unique compound can bloom with scientific light and benefit the world.
    Toxicity Research
    5 - Bromo - 2 - Iodo - 1,3 - Dimethylbenzene Toxicity Study
    Since modern times, chemical substances have been proliferating in the city. 5 - Bromo - 2 - Iodo - 1,3 - Dimethylbenzene is also one of the chemical studies. Those of us who are scholars must investigate its toxicity in depth.
    Looking at the properties of this substance, its molecular structure is unique, and bromine, iodine and dimethyl are combined in the benzene ring. The impact of initial research on organisms should not be ignored. After various experiments, it has been observed that its effect on cells may damage the integrity of cell membranes and disrupt the metabolism in cells.
    In animal experiments, if the mice tested touch this substance, it may be uncomfortable or life-threatening in mild cases, or life-threatening in severe cases. However, the occurrence of its toxicity is closely related to the amount of dose and the duration of exposure.
    We should deeply investigate the reason and understand the cause of its toxicity. When the world uses this substance, we should prevent it from harm, protect the well-being of the people, and protect the purity of the environment. This is the heavy responsibility of our chemical researchers.
    Future Prospects
    I have dedicated myself to the chemical substance 5 - Bromo - 2 - Iodo - 1,3 - Dimethylbenzene. Thinking about its future, the prospect is like the rise of the sun, and it is expected to shine.
    This substance may be the key to organic synthesis. With its unique structure, it can open up new paths of reaction and pave the way for the creation of delicate organic molecules. In the future, it may emerge in the field of drug research and development, helping doctors make special drugs and relieve the pain of patients.
    And it also has potential in the field of materials science. Or it can be turned into a brick and stone for building new functional materials, so that materials have extraordinary properties, such as excellent electrical conductivity and optical properties, which will revolutionize the electronics and optical industries.
    I firmly believe that with time and in-depth research, 5 - Bromo - 2 - Iodo - 1,3 - Dimethylbenzene will be able to demonstrate its endless capabilities, contribute to human well-being and technological progress, and create a brilliant future.
    Where to Buy 5-Bromo-2-Iodo-1,3-Dimethylbenzene in China?
    As a trusted 5-Bromo-2-Iodo-1,3-Dimethylbenzene 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 5-Bromo-2-Iodo-1,3-Dimethylbenzene supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    What is the Chinese name of 5-bromo-2-iodo-1,3-dimethylbenzene?
    5-Bromo-2-iodine-1,3-dimethylbenzene, which is the result of the naming of organic compounds. According to the naming rules of organic compounds, the first look at the substituents, bromine, iodine, and methyl are all common substituents. Take the benzene ring as the parent body and number the carbon atoms on the ring. In order to minimize the sum of the substituent positions, the carbon atoms connected with methyl are numbered 1 and 3 respectively, and then it is determined that bromine is in carbon 5 and iodine is in carbon 2, hence the name. This naming accurately reflects the structure of the compound, which is convenient for chemists to communicate and identify. In its structure, the benzene ring is a stable six-membered ring structure, and methyl (-CH 🥰), bromine atom (-Br), and iodine atom (-I) are respectively connected to the specific position of the benzene ring. Different substituents endow the compound with unique physical and chemical properties. It may have specific uses in organic synthesis and other fields, and its naming lays the foundation for research and application.
    What are the physical properties of 5-bromo-2-iodo-1,3-dimethylbenzene?
    5-Bromo-2-iodine-1,3-dimethylbenzene is one of the organic compounds. Its physical properties are worth exploring, and the details are as follows.
    First of all, under normal temperature and pressure, 5-bromo-2-iodine-1,3-dimethylbenzene is mostly liquid, with a color or nearly colorless, or slightly yellowish, clear and fluid.
    As for its melting and boiling point, the melting point is very low, and it is not solid in ordinary environments. The boiling point is relatively high, due to intermolecular forces. The bromine, iodine atoms and methyl groups in the molecule cause van der Waals forces between molecules, and the electronegativity of the halogen atom is large, which increases the polarity of the molecule, so the boiling point is high.
    In terms of solubility, this compound is extremely insoluble in water. In water, polar solvents are also used, while 5-bromo-2-iodine-1,3-dimethylbenzene molecules have limited polarity and are difficult to dissolve in water according to the principle of "similar miscibility". However, in organic solvents, such as ethanol, ether, and dichloromethane, the solubility is quite good. Because organic solvents are mostly non-polar or weakly polar, they are similar to the intermolecular forces of the compound, so they are miscible.
    Density is also an important physical property. The density of 5-bromo-2-iodine-1,3-dimethylbenzene is greater than that of water. When mixed with water, it will sink to the bottom of the water. This is because the molecule contains bromine and iodine atoms with relatively large atomic mass, resulting in an increase in unit volume mass.
    Volatility, relatively speaking, its volatility is relatively weak. The intermolecular force is large, and it requires more energy to make its molecules leave the liquid phase and enter the gas phase, so it evaporates slowly at room temperature.
    In addition, 5-bromo-2-iodine-1,3-dimethylbenzene may have a certain odor, but the specific odor varies depending on individual olfactory differences, and probably has a special organic odor.
    The above are the common physical properties of 5-bromo-2-iodine-1,3-dimethylbenzene, which are of great significance in the fields of organic synthesis and chemical research, and are related to its separation, purification and application.
    What are the chemical properties of 5-bromo-2-iodo-1,3-dimethylbenzene
    5-Bromo-2-iodine-1,3-dimethylbenzene, an organic compound, has unique chemical properties and is worth studying in depth.
    It has the typical properties of aromatic hydrocarbons, due to the structure of benzene rings. The electron cloud distribution of the benzene ring gives it a certain stability, and it is prone to electrophilic substitution reactions. The π electron cloud of the capped benzene ring is attractive to foreign electrophilic reagents. For example, under certain conditions, it can react with electrophilic reagents such as halogenating agents, nitrifying agents, and sulfonating agents. Taking the halogenation reaction as an example, the hydrogen atom on the benzene ring can be replaced by other halogen atoms to form more complex halogenated aromatic hydrocarbons.
    And because of the substituents such as bromine, iodine and methyl on the benzene ring, these substituents have a significant impact on the electron cloud density and reactivity of the benzene ring. Methyl as the power supply group can increase the electron cloud density of the benzene ring, especially the electron cloud density of the ortho and para-position, which in turn enhances the activity of the electrophilic substitution reaction of the ortho and para-position. Although bromine and iodine are halogen atoms, they have electron-absorbing induction effects, which reduce the electron cloud density of the benzene ring, but also have the effect of electron conjugation. Overall, the electron cloud density of the benzene ring is relatively small, and the degree of reduction of the electron cloud density of the ortho and para-position is less than that of the meta-position, so the electrophilic sub
    In addition, bromine and iodine atoms in this compound are active and can participate in a variety of reactions. If under appropriate conditions, bromine and iodine atoms can be replaced by nucleophiles, and nucleophilic substitution reactions can occur to generate new compounds containing different functional groups. This reaction is of great significance in organic synthesis, and can be used to introduce various functional groups to expand the structure and function of compounds.
    5-Bromo-2-iodine-1,3-dimethylbenzene has a unique structure and rich and diverse chemical properties. It is widely used in organic synthesis, pharmaceutical chemistry and other fields, laying the foundation for the preparation of more complex and functional organic compounds.
    What is the main use of 5-bromo-2-iodo-1,3-dimethylbenzene?
    5-Bromo-2-iodine-1,3-dimethylbenzene is also an organic compound. Its main uses cover the following numbers.
    In the field of organic synthesis, this compound is often an important intermediate. Because of its halogen atoms such as bromine and iodine in the molecule, this halogen atom has good activity and can participate in many organic reactions. Such as nucleophilic substitution reactions, halogen atoms can be replaced by various nucleophiles to form new carbon-heteroatomic bonds, thereby introducing diverse functional groups, paving the way for the synthesis of complex organic molecules. For example, it can react with nucleophiles containing nitrogen, oxygen, sulfur, etc., to obtain corresponding substitution products, which have potential applications in drug synthesis, material chemistry, etc.
    Furthermore, in the field of materials science, it may be introduced into the structure of polymer materials through specific chemical reactions. The presence of bromine and iodine atoms may endow materials with unique physical and chemical properties, such as adjusting the solubility, thermal stability, and optical properties of materials. If it is used in the preparation of photoelectric materials, the electronic effect of halogen atoms may affect the charge transport properties of materials, thereby improving the performance of materials in optoelectronic devices, such as organic Light Emitting Diodes, solar cells, etc.
    In the field of medicinal chemistry, such halogenated aromatic compounds may have certain biological activities. Their structural characteristics may interact with targets in vivo, or they can be used as lead compounds for structural modification and optimization. Through systematic drug R & D process, it is expected to obtain new drugs with specific pharmacological activities and contribute to human health.
    5-bromo-2-iodine-1,3-dimethylbenzene has shown important application value in many fields such as organic synthesis, materials science and medicinal chemistry due to its unique molecular structure, providing rich possibilities for related scientific research and industrial production.
    What are the synthesis methods of 5-bromo-2-iodo-1,3-dimethylbenzene?
    The synthesis of 5-bromo-2-iodine-1,3-dimethylbenzene follows several paths. First, it can be started from a suitable aromatic hydrocarbon. If 1,3-dimethylbenzene is used as a raw material, it should be reacted with a brominating agent. The brominating agent can be selected from bromine ($Br_2 $). Under the catalysis of a suitable catalyst such as iron ($Fe $) or iron tribromide ($FeBr_3 $), the benzene ring of the aromatic hydrocarbon can undergo an electrophilic substitution reaction, and the bromine atom selects the position to obtain 5-bromo-1,3-dimethylbenzene. In this reaction, the catalyst's effect is to polarize the bromine molecule, making it easier to interact with the benzene ring.
    5-bromo-1,3-dimethylbenzene is obtained and then reacted with an iodizing agent. Commonly used iodizing agents such as iodine ($I_2 $) are supplemented with appropriate oxidizing agents such as hydrogen peroxide ($H_2O_2 $) or nitric acid ($HNO_3 $). The function of the oxidizing agent is to oxidize the iodine molecule to a more active iodine positive ion ($I ^ + $), and then electrophilic substitution with 5-bromo-1,3-dimethylbenzene to obtain 5-bromo-2-iodine-1,3-dimethylbenzene.
    Another method can first react with 1,3-dimethyl benzene and an iodizing agent to obtain 2-iodine-1,3-dimethyl benzene according to the above-mentioned similar electrophilic substitution principle. Subsequently, 2-iodine-1,3-dimethyl benzene is treated with a brominating agent, and the target product 5-bromo-2-iodine-1,3-dimethyl benzene can also be obtained by electrophilic substitution reaction.
    In addition, other aromatic hydrocarbons containing specific substituents are used as starting materials, and bromine, iodine and methyl groups are gradually introduced through multi-step reactions to eventually form 5-bromo-2-iodine-1,3-dimethylbenzene. However, such methods are often complicated in steps, and the reaction sequence and conditions need to be carefully planned to achieve the purpose of efficient synthesis. Each method needs to carefully regulate the reaction conditions such as temperature, solvent, and ratio of reactants to obtain products with higher yield and purity.