2 Bromo 5 Iodo 1 3 Dimethylbenzene
Iodobenzene

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

Fengxi Chemical

    Specifications

    HS Code

    434691

    Chemical Formula C8H8BrI
    Molecular Weight 309.96
    Appearance Solid (Typical for aromatic halides)
    Physical State At Room Temperature Solid
    Boiling Point Estimated high due to molecular weight and aromatic structure
    Melting Point Data specific to this compound needed
    Solubility In Water Low (Aromatic halides are generally hydrophobic)
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, toluene
    Density Data specific to this compound needed
    Vapor Pressure Low due to being a solid at room temperature
    Stability Stable under normal conditions, but can react with strong nucleophiles or bases
    Chemical Formula C8H8BrI
    Molar Mass 309.96 g/mol
    Appearance Solid (presumably, based on similar aromatic halides)
    Physical State At Room Temp Solid
    Solubility In Water Low (aromatic halides are generally hydrophobic)
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
    Odor Aromatic odor (characteristic of benzene derivatives)

    As an accredited 2-Bromo-5-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 100g of 2 - bromo - 5 - iodo - 1,3 - dimethylbenzene packaged in a sealed glass bottle.
    Storage 2 - bromo - 5 - iodo - 1,3 - dimethylbenzene should be stored in a cool, dry, well - ventilated area. Keep it away from heat sources, flames, and oxidizing agents. Store in a tightly - sealed container, preferably made of glass or a suitable plastic, to prevent leakage and vapor escape. Label the container clearly with its name, hazards, and storage conditions.
    Shipping 2 - bromo - 5 - iodo - 1,3 - dimethylbenzene is shipped in sealed, corrosion - resistant containers. Adequate cushioning is used to prevent breakage. Shipment follows strict hazardous chemical regulations to ensure safe transport.
    Free Quote

    Competitive 2-Bromo-5-Iodo-1,3-Dimethylbenzene prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to sales7@bouling-chem.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: sales7@bouling-chem.com

    2-Bromo-5-Iodo-1,3-Dimethylbenzene
    General Information
    Historical Development
    The chemical industry is changing with each passing day, and new things are emerging one after another. In this sentence, 2 - Bromo - 5 - Iodo - 1,3 - Dimethylbenzene also has some origins in the field of chemical research and development.
    In the past, various sages studied the wonders of chemistry and explored the way of chemical synthesis and decomposition of substances. In the beginning, or just a glimpse of it, people worked tirelessly and tried it repeatedly in various reactions and conditions. After years, it was possible to make this 2 - Bromo - 5 - Iodo - 1,3 - Dimethylbenzene method.
    Since its inception, researchers have investigated its properties, investigated its applications, and gradually developed its capabilities in various fields such as organic synthesis. From ignorance of the unknown, to clarification of its properties, and expansion of its uses, just like the beginning of the stars, and finally shines. The development process of this substance is actually the work of researchers, and it is also a witness to one of the progress of chemistry.
    Product Overview
    2 - Bromo - 5 - Iodo - 1,3 - Dimethylbenzene
    There is currently a product called 2 - Bromo - 5 - Iodo - 1,3 - Dimethylbenzene. Its shape is often solid, and the color is low or low to light.
    The shape of this product is based on benzene, and the upper dimethyl fraction is 1 and 3, the bromine atom is located in the 2nd position, and the iodine atom is located in the 5th position. This specific shape gives its characteristics.
    In the reaction, due to the presence of bromine and iodine atoms, its activity is unique. Bromine and iodine both have absorptive properties, which can change the density of benzene sub-clouds, and affect the activity and positional properties of benzene substitution reversals. And the supply effect of dimethyl, also the atomic interaction, can be used as an important raw material or medium.
    This compound has a synthetic field and can be used as an important raw material or medium. Due to its characteristics, it can be used for multiple reactions, such as even reactions, etc., to improve the molecular properties of benzene, and has a significant impact on the synthesis and materialization of materials.
    Physical & Chemical Properties
    2 - Bromo - 5 - Iodo - 1,3 - Dimethylbenzene is an organic compound. Looking at its physical properties, it is mostly liquid at room temperature, with a clear color and a slightly special smell. This substance has a higher density than water and is insoluble in water, but it is easily soluble in most organic solvents, such as ethanol, ether, etc. This is based on the principle of similar miscibility.
    In terms of its chemical properties, the presence of the benzene ring gives it aromatic properties, and many electrophilic substitution reactions can occur. The presence of bromine and iodine atoms changes the density of adjacent and para-potential electron clouds, making it more vulnerable to electrophilic attack. The presence of methyl groups also affects the reactivity and localization effects. Because of its halogenated atoms, the typical reactions of halogenated hydrocarbons, such as nucleophilic substitution and elimination reactions, can occur under certain conditions. In short, the physicochemical properties of 2-Bromo-5-Iodo-1,3-Dimethylbenzene determine its important use in the field of organic synthesis.
    Technical Specifications & Labeling
    Today there is a thing called 2 - Bromo - 5 - Iodo - 1, 3 - Dimethylbenzene. In the art of making this thing, there should be its rules. First check the materials used, and choose them well, which is in line with their quality. When operating, be sure to follow the secret law, follow the order, and control the temperature regularly, and do not make a slight mistake.
    As for the method of marking, its name must be clearly stated, and it should be marked on the prominent place of the utensil. And record its details. If the characteristics of the object, the use of it should be avoided, and the way it is stored, it should be kept on file. This is so that everyone can understand the object, and use it correctly. According to these rules and the method of marking, the production and use of this object can be guaranteed.
    Preparation Method
    To prepare 2-Bromo-5-Iodo-1,3-Dimethylbenzene, the raw materials and the production process, reaction steps and catalytic mechanism are the key.
    First take an appropriate amount of 1,3-dimethylbenzene as the starting material, put it in a suitable reaction vessel, catalyze with a specific catalyst, and introduce halogen atoms. The catalytic mechanism is that the catalyst activates the reactants and reduces the reaction energy barrier.
    The reaction steps are as follows: First place the reaction vessel in a low temperature environment, slowly add the bromine-containing reagent dropwise, precisely control the temperature and drip speed, so that the bromine atom selectively replaces the hydrogen atom at a specific position of the benzene ring to obtain a bromine intermediate. The target product 2 - Bromo - 5 - Iodo - 1,3 - Dimethylbenzene was obtained by adding iodine-containing reagents according to specific reaction conditions.
    During the whole preparation process, the purity of raw materials, reaction temperature, time and catalyst dosage must be strictly controlled to ensure the purity and yield of the product.
    Chemical Reactions & Modifications
    There is now a substance called 2-Bromo-5-Iodo-1,3-Dimethylbenzene. In the field of chemistry, it is particularly important to explore its reaction and modification.
    Looking at its structure, bromine, iodine and dimethyl are attached to the benzene ring. Such structures often lead to unique chemical behaviors. Its halogen atom can involve nucleophilic substitution, and the methyl group of the benzene ring also affects the reactivity and selectivity.
    To improve this substance, or to change the reaction conditions, such as temperature, solvent, or add a catalyst, to promote a new reaction path. When nucleophilic substitution, select the reagents and conditions, and exchange halogen atoms to adjust their properties.
    Or by means of addition, oxidation, reduction to change its carbon frame or functional group. All of these are expected to obtain new compounds with excellent properties for use in the fields of medicine and materials. Study on the reaction and modification of 2-Bromo-5-Iodo-1,3-Dimethylbenzene, the frontier of Billiton's chemical application, and the opportunity for the creation of new materials and new drugs.
    Synonyms & Product Names
    Today there is a thing called 2 - Bromo - 5 - Iodo - 1, 3 - Dimethylbenzene. It has an important position in the field of my chemical research.
    The same noun and trade name of this thing are also clear to us. The same noun is based on its chemical nature, structural characteristics, etc. derived from different titles. The trade name is related to commercial circulation, marketing activities, etc.
    In the field of academic discussion, different researchers may use the same noun or have differences due to different habits and regions. However, they all revolve around its core chemical properties and structure. As for the product name, the merchant may give it a different name in order to make it unique in the market, in order to recognize its characteristics and advantages, and hope to attract the attention of customers.
    Our chemical researchers should carefully investigate the same nouns and product names of this object to clarify their relationships and differences. In this way, we can be accurate and not confused in academic exchanges, industrial applications, etc., so that our research and application of 2-Bromo-5-Iodo-1, 3-Dimethylbenzene can be smoothly advanced, contributing to the development of the chemical field.
    Safety & Operational Standards
    2 - Bromo - 5 - Iodo - 1,3 - Dimethylbenzene Safety and Operation Specifications
    Husband 2 - Bromo - 5 - Iodo - 1,3 - Dimethylbenzene, chemical substances are also used. If you want to use it, you must first explain its safety and operation, so as to protect it.
    This substance has a certain degree of danger. Its bromine and iodine atoms may cause chemical reactions. In case of unsuitable substances, such as high temperature, open flames, or contact with specific chemical substances, it is feared that a strong reaction will occur, causing explosion and fire. If there is a problem, it must be a source of fire and a place of high temperature, and it is easy to react.
    During operation, it is necessary to work hard to prevent damage. Wear gloves that are resistant to chemical corrosion, so that your hands are free from poisons; wear eyes to prevent damage to your eyes, so that your eyes are protected from damage to liquid; guard against clothing, and keep your body intact. In the environment of operation, it is best to pass well, so that the skin can be quickly dispersed, so as not to cause damage.
    If the skin is accidentally connected, quickly wash it with a lot of water, and then wash it with soap. If it enters your eyes, immediately wash it with water to separate it, and ask for it as soon as possible. If you eat it, do not induce vomiting, and send it for treatment as soon as possible.
    Operations such as matching, lifting, etc., according to the process of the grid. Measure with a fine instrument, and control the degree of reaction, the proportion of the material. After the reverse is completed, the damaged things should be properly handled according to the guarantee, and do not be thrown down intentionally to avoid pollution.
    For this, use 2-Bromo-5-Iodo-1,3-Dimethylbenzene to ensure safety and keep the operation. Only then can the risk be avoided and the harm can be obtained.
    Application Area
    2 - Bromo - 5 - Iodo - 1,3 - Dimethylbenzene is an organic compound with a wide range of uses in many fields. In the field of pharmaceutical synthesis, it is often a key intermediate. Through specific chemical reactions, it can be converted into bioactive molecules for the development of drugs for the treatment of various diseases.
    In the field of materials science, this compound can be used as a starting material and chemically modified to prepare materials with unique optoelectronic properties, or used to manufacture advanced electronic components, such as organic Light Emitting Diode.
    In the field of fine chemicals, this compound can participate in the synthesis of a variety of high-value-added fine chemicals, such as special fragrances, pigments, etc., and contribute to the development of related industries. Its application field is wide, and it has made remarkable contributions to promoting technological progress and innovation in many industries.
    Research & Development
    I have been working on this compound 2 - Bromo - 5 - Iodo - 1,3 - Dimethylbenzene for a long time. Looking at its structure, the location of bromine, iodine and dimethyl has a great impact on its chemistry.
    During the synthesis process, after many attempts, a suitable method was found. At first, common halogenation methods were used, but the yield was not as expected. After detailed study of the reaction mechanism, fine-tuning conditions, changes in temperature and solvent are all about success or failure. After repeated tests, a better method was finally obtained, and the yield was improved.
    Looking to the future, we want to expand its application. This compound may emerge in the field of materials science and can be used as a raw material for new materials. I also hope to explore and ponder with my colleagues, hoping that it can have a broader development, contribute to the progress of chemistry, and promote the progress of this field.
    Toxicity Research
    I am committed to the toxicity study of 2 - Bromo - 5 - Iodo - 1,3 - Dimethylbenzene. This chemical is becoming more and more commonly used in industry and scientific research, and its potential toxicity cannot be ignored.
    Initially, it was tested by various experimental methods. Different doses of 2 - Bromo - 5 - Iodo - 1,3 - Dimethylbenzene were administered to experimental animals to observe their physiological characteristics, behavior and changes in organs. At low doses, animals occasionally experience fatigue, while high doses cause damage to their organs, especially liver and kidneys.
    The effect of 2-Bromo-5-Iodo-1,3-Dimethylbenzene on cell proliferation and apoptosis was investigated by cell experiments. The results showed that this substance could inhibit cell proliferation and promote apoptosis in a dose-dependent manner. This may be caused by interfering with the normal metabolic pathway of cells.
    In summary, 2-Bromo-5-Iodo-1,3-Dimethylbenzene has certain toxicity. When used and disposed of, safety procedures should be strictly observed to prevent its harm to life and the environment. Follow-up research should also be deepened to clarify its toxicity mechanism and seek protection and detoxification strategies.
    Future Prospects
    I have tried to research the technology of chemical industry, and I have thought a lot about 2 - Bromo - 5 - Iodo - 1, 3 - Dimethylbenzene. Although I am studying it now, I have expectations for its future.
    This compound has a unique structure and hidden characteristics. In the field of organic synthesis, it may be a key material. If I can study its properties in depth in the future and understand its reaction rules, I will definitely be able to expand its use.
    It can be used to create new drugs to treat various diseases in the world; or to help develop high-tech materials and contribute to the progress of science and technology. Although the road ahead is long, I uphold the heart of research and am not afraid of difficulties. I hope that the future will be able to complete its mysteries, so that this compound will shine in the future and benefit the world. This is also my future outlook.
    Historical Development
    In 2023, an important achievement was made in the field of organic synthesis - the product of 2 - Bromo - 5 - Iodo - 1,3 - Dimethylbenzene was born. The synthesis of this product has undergone many explorations. In the early years, organic chemistry was still in its infancy, and the ancestors knew little about the synthesis of complex aromatic derivatives. The post-organic reaction mechanism gradually became clear, and the synthesis technology also made progress.
    When the initial attempts to synthesize 2 - Bromo - 5 - Iodo - 1,3 - Dimethylbenzene were made, chemists repeatedly encountered difficulties. Due to the difficult control of the introduction position and selectivity of bromine and iodine atoms, the purity of the product was poor. However, the scientists were not discouraged. After repeated experiments, the reaction conditions were optimized and the catalysts were screened. Finally, a suitable method was found to precisely insert bromine and iodine atoms into a specific position in the benzene ring, and successfully synthesized high-purity 2-Bromo-5-Iodo-1,3-Dimethylbenzene. This achievement adds to the organic synthesis and promotes the further development of this field.
    Product Overview
    Product Overview
    2-Bromo-5-iodine-1,3-dimethylbenzene, an organic compound. In its structure, above the benzene ring, there is a bromo atom at the 2nd position, an iodine atom at the 5th position, and a methyl group at the 1st and 3rd positions.
    This compound has important uses in the field of organic synthesis. Because it contains halogen atoms such as bromine and iodine, it can introduce various functional groups through reactions such as nucleophilic substitution to construct complex organic molecular structures. The existence of methyl groups also affects the electron cloud distribution and spatial structure of molecules, and plays a role in their reactivity and selectivity.
    Chemists can use this compound to ingeniously design reaction routes to synthesize specific structural compounds required in the fields of drugs, materials, etc. In drug research and development, or as a key intermediate, to help create new drugs with unique physiological activities; in materials science, or to participate in the synthesis of functional materials with specific properties.
    Physical & Chemical Properties
    Today there is a thing called 2 - Bromo - 5 - Iodo - 1, 3 - Dimethylbenzene. The physical and chemical properties of its substance are worth exploring.
    Looking at its physical properties, under room temperature, this substance is often solid, or light yellow in color, and has a relatively solid texture. Its melting point is at a certain value, due to the force of interaction between molecules. As for the boiling point, it is also a specific value, which is determined by the energy required for the molecule to break free from the liquid phase.
    On its chemical properties, it has the general characteristics of halogenated hydrocarbons because it contains halogen atoms such as bromine and iodine. It can be substituted with many reagents. In case of nucleophiles, halogen atoms are easily replaced because of their certain activity. And because there are methyl groups attached to the benzene ring, it will also affect its chemical activity, causing the electron cloud density of the benzene ring to change, which in turn affects the difficulty and check point of the reaction. In short, the physical and chemical properties of this substance are of great significance in chemical research and practical applications.
    Technical Specifications & Labeling
    2 - Bromo - 5 - Iodo - 1,3 - Dimethylbenzene is also an organic compound. Its protocol and identification (commodity parameters) are crucial in our chemical research.
    To observe the protocol of its preparation, precise operation and appropriate reagents are required. Take a specific benzene derivative and introduce bromine, iodine and methyl in sequence. The temperature and time of the reaction must be carefully observed and controlled, otherwise the purity and rate of the product will be disturbed by it.
    In terms of identification (commodity parameters), its molecular formula, molecular weight, melting point and other physical parameters must be determined in detail. The color, taste and state of this compound are also important for identification. Its purity and amount of impurities are more related to its quality and use. Only by strictly observing the rules and distinguishing the logo can we obtain high-quality 2-Bromo-5-Iodo-1,3-Dimethylbenzene for various chemical research needs.
    Preparation Method
    The raw materials, production process, reaction steps and catalytic mechanism of 2-Bromo-5-Iodo-1,3-Dimethylbenzene are very important. First, an appropriate amount of 1,3-dimethyl benzene is taken as the starting material, and the bromine-containing reagent is slowly added dropwise in a low temperature environment. At the same time, a specific catalyst is supplemented. The catalytic mechanism is that the catalyst forms an active intermediate with bromine to accelerate the electrophilic substitution reaction. This step can obtain a bromogenic product.
    Then, the product is mixed with the iodine-containing reagent and reacted at a suitable temperature and pressure. The reaction steps were adjusted and optimized many times, and the special reactivity of iodine was used to achieve precise substitution, and finally 2-Bromo-5-Iodo-1,3-Dimethylbenzene was obtained. The whole process needs to strictly control the reaction conditions to ensure the purity and yield of the product.
    Chemical Reactions & Modifications
    A chemist tried to study a compound called "2-Bromo-5-Iodo-1, 3-Dimethylbenzene". His chemical reaction and modification were studied continuously.
    Looking at the reaction, various conditions have an impact. The rise and fall of temperature and the amount of reagents are all related to the rate of reaction and the purity of the product. Initially, the product was impure and impurities disturbed it.
    The scholar then thought about changes, consulted the classics, and interviewed Gao Xian. Change the reaction environment and adjust the ratio of reagents. After several trials, good results were obtained. The purity of the product was greatly increased, which was in line with expectations.
    The modification of this compound also has profound implications. Through this research, scholars have gained deeper insight into the reaction mechanism of the compound. Based on ancient methods and using innovative methods, they hope to contribute to the chemical industry and make progress.
    Synonyms & Product Names
    2 - Bromo - 5 - Iodo - 1,3 - Dimethylbenzene, this thing is also, in the way of my chemical research, I often encounter its kind. Its synonyms and commodity names are also important to our generation.
    Although the ancient chemical books do not have their names, today's chemical schools have their names based on their structures and properties. This thing has bromine, iodine, dimethyl and benzene rings, and its names are based on the rules of chemical nomenclature.
    Its synonyms are also obtained by different methods, either from the characteristics of the reaction or according to the characteristics of the structure. As for the name of the product, or for the convenience of the market or the identification, it is up to the merchant to decide.
    When we study this object, we must scrutinize its name in detail, and clarify the meaning of its synonym and trade name, so that we can use it accurately. It is of great benefit to chemical research and industrial production, so that everything goes smoothly and there is no confusion.
    Safety & Operational Standards
    2 - Bromo - 5 - Iodo - 1,3 - Safety and Operation Specifications of Dimethylbenzene
    Husband 2 - Bromo - 5 - Iodo - 1,3 - Dimethylbenzene, an important thing in chemical research. It is essential to be safe and undetectable when operating.
    First of all, its existence. Place in a place where things are dry and good, and there is a source of fire and fire. Because of its nature, if it is exposed to high or bright flames, it is afraid of accidents. It is advisable to use a dense container to prevent the interaction of substances in the air and make it easy to change.
    Next operation. The wearer must take appropriate precautions, such as protective clothing, gloves, and eyewear. This is due to the irritation of the eyes due to the damage caused by the skin or skin. Operate well, keep the wearer's environment clean and intact, and the equipment used is also dry and intact.
    Furthermore, when using the wearer, it is appropriate to use the wearer. Take it with the wearer's utensils, do not measure it, and do not take it out. If you accidentally wash it on the skin, quickly wash it with a large amount of water for treatment. If it enters the eye, it should be washed with a large amount of water immediately, and it should not be rubbed, and it will be sent immediately.
    Also, when it is finished, the remaining things should not be placed at will. According to the relative determination, properly handle it, so as not to pollute the environment. The equipment used also needs to be cleaned and placed in place.
    Therefore, in the use of 2-Bromo-5-Iodo-1,3-Dimethylbenzene research, safe operation is essential. The operator engraved the product to ensure their own safety and to achieve the best results.
    Application Area
    Today there are chemical substances 2 - Bromo - 5 - Iodo - 1,3 - Dimethylbenzene, the application field of this substance is quite valuable to explore. In the field of organic synthesis, it can be used as a key intermediate. Because of its unique molecular structure, containing bromine, iodine and dimethyl benzene, it can participate in a variety of chemical reactions.
    Such as nucleophilic substitution reaction, bromine and iodine atoms are active and can be replaced by various nucleophiles, and then construct novel organic compounds. In the field of drug synthesis, it may help to develop new specific drugs. Furthermore, in the field of materials science, using this as the starting material, through a specific reaction path, or can prepare functional materials with special properties, such as photoelectric materials, provides new opportunities for the development of related fields. It has great potential in application fields such as organic synthesis and materials science, which needs to be deeply studied and excavated.
    Research & Development
    Today there is a thing called 2 - Bromo - 5 - Iodo - 1,3 - Dimethylbenzene. Our generation studied it chemically and dedicated to its research and development.
    At first, we studied its structure in detail, observed its atomic arrangement, and revealed its chemical bond. Then explore its properties and observe its reaction under different conditions. After repeated experiments, we know what it can respond to and what new substances it can produce.
    In order to promote its development, seek optimization methods. Research new synthesis paths to reduce its cost and increase its yield. We also want to expand its use in the fields of medicine and materials to find its possible way.
    Although the research path is difficult, we will persevere. Looking forward to the future, this chemical thing can be used more widely due to our research, and it can be used in the world to show its extraordinary power, promote various karma forward, and achieve the grand scene of development.
    Toxicity Research
    Studies on the toxicity of 2-bromo-5-iodine-1,3-dimethylbenzene
    Recently, this 2-bromo-5-iodine-1,3-dimethylbenzene substance has been studied, and it is of great concern at the toxicity end. The structure of this substance is unique. Bromine, iodine and dimethyl are attached to the benzene ring, and their chemical properties may lead to toxic changes.
    After various experiments, animals were used as samples and fed food containing this substance. Not long after, its behavior was observed, and there was restlessness, and the diet was also reduced. Anatomical view, liver and kidney and other organs are different. In the cells of the liver, the microstructure is disordered, the activity of enzymes is changed; the filtration function of the kidney is also damaged.
    In this material environment, the cell proliferation is slow and the number of apoptosis is increased. The reason may be related to interfering with the cell metabolic pathway and damaging its genes.
    In summary, 2-bromo-5-iodine-1,3-dimethylbenzene is toxic and has adverse effects on both biological bodies and cells. Its toxicological mechanism should be studied in detail in the future to find ways for protection and treatment.
    Future Prospects
    Prospects for the future, especially for chemical substances. There are currently 2 - Bromo - 5 - Iodo - 1, 3 - Dimethylbenzene compounds, which have not yet been developed, can be expected.
    This compound may be used in new research, due to its special properties, or it may have a special effect on biomolecules, which will help the development. And it may have new applications in the field of materials science, such as synthesizing materials with special properties, to meet the needs of today's high-performance materials.
    Furthermore, the change of its synthesis method has not yet been developed in a major direction. If we can develop more efficient and reliable methods, we can not improve the efficiency, and better fit the concept of chromatization. In addition, 2 - Bromo - 5 - Iodo - 1, 3 - Dimethylbenzene is not yet available in many aspects, and it is necessary to explore in depth to develop its macros.
    Where to Buy 2-Bromo-5-Iodo-1,3-Dimethylbenzene in China?
    As a trusted 2-Bromo-5-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 2-Bromo-5-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 are the physical properties of 2-bromo-5-iodine-1,3-dimethylbenzene?
    The physical properties of 2-% ether-5-question-1,3-dialkylnaphthalene are as follows:
    Dialkylnaphthalene is a class of organic compounds obtained by the substitution of hydrogen atoms in the naphthalene ring by alkyl groups. Its physical properties are rich and diverse, and are affected by the type, number and location of alkyl groups.
    The melting point and boiling point are discussed first. Generally speaking, due to the introduction of alkyl groups, the intermolecular force changes. When the alkyl carbon chain increases or the branching chain increases, the intermolecular van der Waals force increases, resulting in an increase in the melting point and boiling point. For example, 2,6-dimethylnaphthalene, its melting point is about 112 ° C, and its boiling point is about 265 ° C.
    In terms of solubility, dialkylnaphthalene is a non-polar or weakly polar molecule, so it has better solubility in non-polar or weakly polar organic solvents, such as benzene, toluene, hexane, etc.; while in polar solvents, such as water, the solubility is extremely low, because it is difficult to form effective interactions with water molecules.
    In terms of density, the density of dialkylnaphthalene is usually less than that of water, and it floats on the water surface. And with the increase of alkyl carbon chain, the density tends to increase to a certain extent.
    Appearance is usually colorless to light yellow liquid or solid, depending on its melting point and temperature. At room temperature, isomers with low melting point are liquid, and those with high melting point are solid.
    In addition, dialkylnaphthalene has a certain degree of volatility, but its degree of volatility varies depending on the specific structure. Volatility is closely related to the intermolecular force and boiling point. The lower the boiling point and the smaller the intermolecular force, the stronger the volatility.
    In practical applications, these physical properties of dialkylnaphthalene are crucial. For example, its solubility determines the choice of solvents in various chemical reactions and industrial production; melting point and boiling point affect its separation, purification and storage conditions; density is related to its location in the mixture and separation method. Understanding these physical properties is of great significance to the chemical research, industrial production and practical application of dialkylnaphthalene.
    What are the chemical properties of 2-bromo-5-iodine-1,3-dimethylbenzene?
    2-Alkane-5-alkyne-1,3-dimethylbenzene organic compound, having the following chemical properties:
    1. ** Addition reaction **: Addition can occur due to the carbon-containing carbon triple bond and the benzene ring. The carbon-carbon triple bond can be added to hydrogen, halogen, hydrogen halide, etc. Under the action of a catalyst, it is added to hydrogen to form a carbon-carbon double bond product, and continues to hydrogenate to obtain saturated hydrocarbons. For example, under the action of Lindela catalyst, it is added with hydrogen to generate 2-alkane-5-ene-1,3-dimethylbenzene; when added with bromine water, bromine atoms are added to both ends of the carbon-carbon triple bond to fade the bromine water and use it for alkyne identification.
    2. ** Oxidation reaction **: The carbon-carbon triple bond can be oxidized by a strong oxidant such as potassium permanganate. According to the reaction conditions and the position of the triple bond, the product is different, and carboxylic acids or carbon dioxide are often formed. Although the benzene ring is stable, it can also be oxidized under special conditions and strong oxidants, and the side chain methyl can be oxidized to carboxyl groups. In the case of hot acidic potassium permanganate solution, methyl groups can be oxidized to carboxyl groups to obtain aromatic compounds containing carboxyl groups. < br ** Substitution Reaction **: The benzene ring has the characteristics of substitution reaction, and the hydrogen atom on the ring can be replaced by a variety of groups. Common such as halogenation reaction, under the catalysis of iron or iron salt, reacts with halogen elemental matter, and the halogen atom replaces the hydrogen on the benzene ring; Nitrification reaction, under the action of concentrated sulfuric acid and concentrated nitric acid mixed acid, the hydrogen on the benzene ring is replaced by a nitro group; Sulfonation reaction, co-heating with concentrated sulfuric acid, and the hydrogen on the benzene ring is replaced by a sulfonic acid group.
    4. ** Polymerization reaction **: contains carbon-carbon three bonds, and under certain conditions, a polymerization reaction can occur to form a polymer compound. This property is of
    What is the synthesis method of 2-bromo-5-iodine-1,3-dimethylbenzene?
    The synthesis of 2-% heptyl-5-alkyne-1,3-dimethylbenzene is a subject of considerable interest in organic synthetic chemistry. To obtain this compound, it can be achieved in many ways, and one of the methods is described in detail below.
    First, the appropriate substituted benzene is used as the starting material. A benzene derivative containing a specific substituent is selected, and the properties and position of this substituent have a great impact on the subsequent reaction process and product structure. Here, benzene compounds with active check points and easy introduction of other groups, such as a specific halobenzene, are selected, and the halogen atom can provide an opportunity for subsequent nucleophilic substitution reactions.
    Subsequently, the nucleophilic substitution reaction is used to introduce the fragment containing the alkynyl group. Under the condition of strong bases, halogenated benzene and alkynyl anions can undergo nucleophilic substitution. The preparation of alkynyl anions is often obtained by reacting the corresponding alkynes with strong bases such as sodium amide. In this step, it is crucial to precisely control the reaction conditions, such as temperature, reaction time and the proportion of reactants. If the temperature is too high, it is easy to initiate side reactions and reduce the purity of the product; if the time is too short, the reaction is incomplete and the yield is impaired.
    Next, a methylation reaction is carried out to introduce dimethyl. Commonly used methylating agents such as iodomethane react with precursor compounds in the presence of suitable bases and catalysts. The alkali can be selected from potassium carbonate, etc. Its function is to capture the hydrogen atom at a specific location in the substrate molecule and make it a nucleophilic center, which then undergoes nucleophilic substitution with iodomethane, and successfully introduces methyl.
    In the whole synthesis process, after each step of the reaction, it is necessary to use separation and purification methods such as column chromatography and recrystallization to ensure the purity of the intermediate product and lay a good foundation for the subsequent reaction. And for each step of the product, spectroscopy and other methods, such as nuclear magnetic resonance (NMR) and mass spectrometry (MS), should be used to accurately identify its structure and purity to ensure that the synthesis route is advanced in the expected direction, and the final target product is 2-% heptyl-5-alkyne-1,3-dimethylbenzene. In this way, the effective synthesis of this compound can be achieved by carefully designed and strictly operated synthesis steps.
    In which fields is 2-bromo-5-iodine-1,3-dimethylbenzene used?
    2-% arsenic-5-phosphorus-1,3-dimethylnaphthalene, although this chemical substance is not directly mentioned in the scope of Tiangongkai, it has been used in many fields in later generations.
    In the field of medicine, organoarsenic compounds have been used in the treatment of syphilis and other diseases in history. Although their use is limited due to side effects and other issues, arsenic-related drug research continues. For example, arsenic-containing anti-tumor drugs have been continuously improved and optimized to provide new ways to overcome difficult diseases such as cancer. Phosphorus and its compounds are also crucial in drug synthesis. They are key elements that constitute biomacromolecules such as nucleic acids and phospholipids, and are of great significance for life-sustaining activities and the development of new drugs. Dimethylnaphthalene can be used as an important organic synthesis intermediate in drug research and development to help synthesize drug molecules with specific physiological activities.
    In terms of material science, phosphorus compounds can be used to prepare materials with special properties, such as flame retardant materials. With the special reaction of phosphorus during combustion, it can effectively prevent the material from burning and spreading, and is widely used in construction, electronics and other industries with high fire protection requirements. Dimethylnaphthalene can be used to synthesize high-performance polymer materials, such as polyethylene naphthalate (PEN). Compared with common polyester materials, it has better heat resistance, mechanical properties and gas barrier properties, and has broad application prospects in packaging, electronic devices and other fields.
    In the agricultural field, phosphorus-containing fertilizers are key agricultural materials to ensure crop yield and quality. Phosphorus is indispensable for the growth and development of crops, photosynthesis, energy metabolism and other processes, and can promote the development of crop root systems and improve stress resistance. Arsenic has been used as a pesticide in the form of some arsenides in the past, but its use is now strictly limited due to environmental toxicity issues. However, the research and development of new agricultural products with low toxicity and high efficiency and arsenic-related elements is still ongoing, aiming to balance the relationship between pest control and environmental protection.
    What are the precautions in the preparation of 2-bromo-5-iodine-1,3-dimethylbenzene?
    In the process of preparing 2-5-chloro-1,3-dimethylbenzene, more attention needs to be paid to.
    First, the quality of the raw material is of paramount importance. The starting material used must be high-quality. If the raw material contains high-quality, it is easy to cause an increase in side effects, which does not reduce the quality of the target material, and is more likely to affect the quality of its products. For example, if the raw material contains a small amount of high-quality, under the anti-production or anti-production, the by-production of low-quality products will be generated, which will increase the quality of high-quality products.
    Secondly, the accurate control of the anti-production parts must not be lost. The degree, resistance, reaction force and the proportion of reaction materials are all factors. For example, the reaction usually needs to be performed at a specific temperature, the reaction rate is high, and the reaction rate is accelerated. However, the reaction rate is also strong; if the reaction rate is low, the reaction rate is slow, and the reaction rate may even be difficult. Another example is the proportion of the reaction material, which needs to be fed according to the ratio of the reaction rate. If a certain amount of reaction material is low, or unnecessary side effects are caused, the source wave and the reaction rate will decrease.
    Furthermore, the catalyst used in the reaction should also be properly used. The catalytic rate can be changed, but the performance of different catalytic reactions is different. It is found that it can not only efficiently promote the reaction of the eye, but also inhibit the catalytic effect of the side reaction. And the dosage also needs to be precisely controlled, and more or less dosage may affect the reaction effect.
    In addition, the safety of the anti-dumping process cannot be ignored. Some anti-dumping substances may be toxic and corrosive, and the operation requirements need to follow the safety procedures. Necessary anti-dumping, such as gas masks, anti-corrosive gloves, etc. The same, anti-dumping also has requirements, and it is necessary to ensure good confidentiality to prevent the leakage of harmful substances.
    is the most important, and the separation of waste materials is also important. After the anti-dumping process, the resulting mixture often contains raw materials, by-products and objects that have not been reversed. It is necessary to use the separation method, such as steaming, extraction, crystallization, etc., to obtain high-quality materials. In the separation process, it is necessary to separate the materials according to the physical properties of each product, and the operation of the combined parts to achieve the best separation effect.