2 Bromo 1 Iodo 3 Methylbenzene
Iodobenzene

2-Bromo-1-Iodo-3-Methylbenzene

Fengxi Chemical

    Specifications

    HS Code

    328719

    Chemical Formula C7H6BrI
    Molecular Weight 283.93
    Appearance Solid (likely)
    Solubility In Water Low (organic aromatic halide, non - polar nature)
    Solubility In Organic Solvents Good (in common organic solvents like ethanol, ether)
    Stability Stable under normal conditions but reactive to strong bases and reducing agents
    Chemical Formula C7H6BrI
    Molar Mass 297.93 g/mol
    Appearance Solid (presumably, based on similar aromatic halides)
    Physical State At Room Temp Solid
    Solubility In Water Insoluble (aromatic halides are generally hydrophobic)
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
    Stability Stable under normal conditions, but may react with strong bases, reducing agents etc.

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

    Packing & Storage
    Packing 500g of 2 - bromo - 1 - iodo - 3 - methylbenzene packaged in a sealed glass bottle.
    Storage 2 - bromo - 1 - iodo - 3 - methylbenzene should be stored in a cool, dry, well - ventilated area away from heat sources and open flames. It should be kept in a tightly - sealed container to prevent evaporation and exposure to air or moisture. Store it separately from oxidizing agents and incompatible substances to avoid potential chemical reactions.
    Shipping 2 - bromo - 1 - iodo - 3 - methylbenzene is shipped in sealed, corrosion - resistant containers. It's transported under regulated conditions, avoiding heat and direct sunlight, with proper hazard labels to ensure safe transit.
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    2-Bromo-1-Iodo-3-Methylbenzene
    General Information
    Historical Development
    Fu 2 - Bromo - 1 - Iodo - 3 - Methylbenzene has gradually emerged in the field of chemistry. Back in the beginning, early chemists studied the way of organic synthesis and dedicated themselves to expanding the variety of compounds.
    At that time, organic synthesis was still in its infancy, and many wise men explored the secret of material synthesis with their perseverance and wisdom. After years of hard work, the understanding of halogenated aromatics has gradually deepened, so there is an attempt to synthesize 2 - Bromo - 1 - Iodo - 3 - Methylbenzene.
    At the beginning, the synthesis method was simple and the yield was quite low, but scholars were not discouraged. As the years passed, the chemical theory became more and more complete, and the experimental skills became more and more exquisite. New reaction mechanisms were solved, and efficient catalysts were developed. The method of synthesizing this compound became more and more mature, and the yield and purity increased.
    Looking at its development path, it is like a boat going against the water, making unremitting progress. The difficulties and obstacles of the past have turned into a smooth road for the present. 2 - Bromo - 1 - Iodo - 3 - Methylbenzene has also been widely used in medicine, materials and other fields, contributing to the rise of science and technology.
    Product Overview
    Today there is a substance called 2 - Bromo - 1 - Iodo - 3 - Methylbenzene. It is an organic compound with a unique structure. Looking at its structure, above the benzene ring, the bromine atom is in two positions, the iodine atom is in one position, and the methyl is in three positions. The properties of this compound are determined by the arrangement and bonding of its atoms.
    Its physical properties, at room temperature, are either solid or liquid, depending on environmental conditions. Its melting and boiling point varies depending on the force between molecules. Chemical properties are active and can participate in many reactions. Due to the presence of halogen atoms, nucleophilic substitution reactions are prone to occur, and benzene rings can also carry out various aromatic reactions.
    In the field of organic synthesis, this compound has a wide range of uses. It can be used as an intermediate to prepare complex organic molecules. Through ingenious reaction design, different functional groups can be introduced to expand their chemical derivation pathways. Researchers can use this material to explore new synthesis routes and develop materials with special properties, which have potential application value in many fields such as medicine and materials science.
    Physical & Chemical Properties
    2 - Bromo - 1 - Iodo - 3 - Methylbenzene is an organic compound. In terms of physical properties, it is mostly liquid at room temperature, has a certain volatility, and can emit a specific odor in the air. Its boiling point is related to the intermolecular force. Due to the introduction of bromine and iodine atoms, the intermolecular force is enhanced, and the boiling point is higher.
    Chemically, the benzene ring endows it with aromatic properties and can undergo electrophilic substitution reactions. Bromine and iodine atoms are ortho-para-site groups, which increase the density of the ortho-para-site electron cloud of the benzene ring, which is conducive to the attack of electrophilic reagents. Methyl is also a power supply group, which has an impact on the reactivity. This compound can participate in the common reactions of halogenated hydrocarbons, such as the substitution reaction with nucleophiles, and the bromine and iodine atoms can be replaced by other groups, which is widely used in the field of organic synthesis.
    Technical Specifications & Labeling
    2 - Bromo - 1 - Iodo - 3 - Methylbenzene is an organic compound. It is related to the technical specifications and identification (product parameters) of this compound. Let me tell you in detail.
    Looking at its technical specifications, this compound must have high purity and the impurity content must be strictly controlled. Its physical properties also need to be stable, such as melting point, boiling point and other parameters, when within a specific range. During the production process, the reaction conditions need to be precisely controlled, such as temperature, pressure, reaction time, etc., which will affect the purity and yield of the product.
    As for the label (product parameters), the chemical name "2 - Bromo - 1 - Iodo - 3 - Methylbenzene" should be clearly marked on the label, and key information such as chemical formula and molecular weight should be noted. At the same time, the warning label is also indispensable to clarify the possible danger and ensure the safety of user operation. In this way, you can get 2 - Bromo - 1 - Iodo - 3 - Methylbenzene products with high quality and clear labels.
    Preparation Method
    The method of making 2 - Bromo - 1 - Iodo - 3 - Methylbenzene should be investigated in detail.
    The selection of raw materials should start with 3 - methylaniline. First, it should be combined with an appropriate amount of bromine water to obtain 2 - bromo - 3 - methylaniline. This step needs to be controlled at temperature, and it should not be overly dramatic or cause other heterogeneity.
    Next, take the obtained 2 - bromo - 3 - methylaniline, co-place it with iodine and an appropriate oxidant, and change it through oxidation and rearrangement to form 2 - Bromo - 1 - Iodo - 3 - Methylbenzene. During the reaction process, it is advisable to observe the situation frequently, adjust the temperature and the amount of agent in a timely manner.
    As for the catalytic mechanism, the oxidant initiates the transition of electrons, causing the radical change of aniline, and the bromine and iodine are sequentially put into place, which is the required material. After each step of the reaction, the production is refined, and the impurities are removed and purified to achieve high purity.
    Chemical Reactions & Modifications
    The wonders of chemistry lie between reaction and modification. In today's discussion of 2 - Bromo - 1 - Iodo - 3 - Methylbenzene, the change of its reaction is worth exploring.
    In past studies, it has been seen that the halogenation reaction, the position of bromine and iodine, affects the molecular activity. If you want to change its properties, you can apply different conditions. Changing the temperature or changing the solvent can make the reaction different. Raising the temperature increases the reaction rate, but the selectivity or decreases. And with a specific solvent, such as non-polar ones, it may be able to direct a specific product.
    When modified, new groups can be introduced. After nucleophilic substitution, with suitable nucleophilic reagents, halogen atoms can be substituted to make molecules have new characteristics. This is all a way for chemists to explore, by means of reactions, to change the properties of substances to meet the needs of diversity.
    Synonyms & Product Names
    Today there is a thing named 2 - Bromo - 1 - Iodo - 3 - Methylbenzene. This thing is quite important in my chemical research. Its synonymous name is also of concern to researchers.
    In the field of Guanfu chemistry, it is common to have more than one thing. 2 - Bromo - 1 - Iodo - 3 - Methylbenzene may have another name for its chemical structure characteristics. The reason for this is that due to the variety of chemical naming rules, the same substance can be called differently under different systems.
    As for the product name, merchants will also give it a unique name in order to highlight their characteristics or facilitate market circulation. Either take its performance, or according to its use, each has its own consideration. Although the names of such synonyms and trade names are different, they all refer to this thing. For our researchers, it is clear that many of their terms can be used in academic exchanges and experimental research without the risk of confusion, and the investigation of 2-Bromo-1-Iodo-3-Methylbenzene can be smoothly advanced.
    Safety & Operational Standards
    2 - Bromo - 1 - Iodo - 3 - Methylbenzene Safety and Operation Specifications
    Fu 2 - Bromo - 1 - Iodo - 3 - Methylbenzene is a compound commonly used in chemical research. If you want to use this product, the first priority is safety, and the operation specifications can be followed to ensure the smooth operation of the experiment and the safety of personnel.
    Safety is the most important thing. This product has certain chemical activity or is harmful to the human body. When operating, you must wear protective equipment, such as gloves, goggles, protective clothing, etc., to prevent it from contacting the skin and eyes. Its odor may be irritating, and it is suitable for operation in a well-ventilated place. If it is in a confined space, harmful gases will accumulate, which may harm the respiratory system.
    Furthermore, attention should also be paid to storage. It should be placed in a cool and dry place, away from fire and heat sources, and away from direct sunlight. Due to its chemical properties or reaction with other things, it should not be co-stored with oxidants, strong acids, strong alkalis, etc., to prevent accidental changes.
    Operating specifications should not be ignored. When taking it, use clean and dry utensils, and take it accurately according to the experimental requirements. Do not touch it with your bare hands to avoid poisoning. If it is accidentally splashed on the skin, rinse it with a lot of water quickly, and seek medical attention for those who are serious.
    The reaction process requires strict temperature control, time control, and operation according to the chemical reaction mechanism. After the experiment, properly dispose of the remaining materials, do not dump them at will, and dispose of them according to environmental protection requirements, so as to avoid polluting the environment.
    In general, in the research and use of 2 - Bromo - 1 - Iodo - 3 - Methylbenzene, safety and operating standards are the top priority. Only by strictly observing these two can we move forward steadily on the road of chemical exploration, avoid disasters, and achieve the purpose of scientific research.
    Application Area
    The application field of 2 - Bromo - 1 - Iodo - 3 - Methylbenzene
    There are chemical substances 2 - Bromo - 1 - Iodo - 3 - Methylbenzene, which are used in various fields. In the field of organic synthesis, this compound can be a key intermediate. Because its structure contains bromine, iodine and methyl, it can be used for many chemical reactions, such as nucleophilic substitution, coupling reactions, etc., to prepare various complex organic molecules.
    In the field of pharmaceutical chemistry, using it as a starting material, through delicate synthesis steps, compounds with specific biological activities can be prepared, or the foundation for the development of new drugs can be laid. Furthermore, in the field of materials science, by chemically modifying it, or materials with special photoelectric properties can be prepared, which can be used in organic Light Emitting Diodes, solar cells and other devices, providing possibilities for material innovation.
    In summary, although 2 - Bromo - 1 - Iodo - 3 - Methylbenzene is an organic compound, it has unlimited potential in organic synthesis, pharmaceutical chemistry, materials science and other application fields, waiting for researchers to further explore and develop.
    Research & Development
    In modern times, chemistry has advanced, and the research of substances has become increasingly prosperous. Today there is 2 - Bromo - 1 - Iodo - 3 - Methylbenzene, and our generation has devoted himself to studying it.
    Study its synthesis method, explore the mechanism of various reactions, and strive for ingenuity and efficiency. After repeated tests, or find a good way, the yield will gradually increase.
    Observe its properties, observe its changes under different media and conditions. Understand its chemical activity and lay the foundation for its application.
    As for development, I hope it can emerge in the fields of medicine and materials. With its characteristics, it helps the precision of pharmaceutical research and development and promotes the improvement of material properties. We should make unremitting efforts to study it, hope it will flourish, be used by the world, and benefit people.
    Toxicity Research
    Toxicity Study of 2 - Bromo - 1 - Iodo - 3 - Methylbenzene
    I am committed to the toxicity study of 2 - Bromo - 1 - Iodo - 3 - Methylbenzene. This chemical is occasionally used in industry and scientific research, but its toxicity has rarely been carefully observed in the past.
    I have used various experimental methods to study its effects on organisms. At first, small animals were used as samples to observe the physiological changes after ingesting this substance. Looking at their behavior, the tested animals showed signs of fatigue and loss of appetite. Then examining their organs, it was found that the liver and kidneys were damaged to varying degrees. The structure of liver cells is disordered, and the filtering function of the kidneys is also abnormal.
    The direct effect of this substance on cells was investigated by cell culture. The results showed that it can inhibit cell proliferation and induce apoptosis. Analyze its mechanism, which may be related to interfering with intracellular signaling pathways.
    In summary, 2-Bromo-1-Iodo-3-Methylbenzene has certain toxicity. When using and disposing, care should be taken to prevent it from causing harm to organisms and the environment.
    Future Prospects
    The product of Guanfu chemistry, 2 - Bromo - 1 - Iodo - 3 - Methylbenzene, has extraordinary potential. In the future development, it is expected to shine in the field of materials science. Or with its unique structure, it can develop new materials with excellent performance, reduce weight and increase efficiency for electronic devices, and make portable devices more delicate.
    Furthermore, in the field of medicinal chemistry, it also holds infinite possibilities. Through exquisite synthesis methods, it may be able to derive special drugs to fight against various difficult diseases and save people from illness.
    With the field of organic synthesis in mind, as a cornerstone, novel reaction paths can be expanded, synthesis strategies can be enriched, and the building block of organic chemistry can be added. Our generation of chemical researchers should study diligently, hoping to develop their potential, so as to promote the progress of science and technology, seek the well-being of mankind, and make the future scene as colorful as spring flowers.
    Historical Development
    About the historical development of 2 - Bromo - 1 - Iodo - 3 - Methylbenzene (classical Chinese fragment)
    Ancient chemistry began to rise, and sentient beings paid attention to the changes of matter. And in modern times, research has become more and more refined, and many new qualities have appeared in the world. 2 - Bromo - 1 - Iodo - 3 - Methylbenzene is also one of the things studied in chemistry.
    At the beginning, all the sages observed the changes of the organic, and explored the details. Some wise people paid attention to the derivation of aromatic rings, and wanted to study their properties with halogenated substances. After years of work, various techniques advanced day by day. First there was the method of bromide substitution, followed by iodine substitution. With the combination of the two, the compound 2 - Bromo - 1 - Iodo - 3 - Methylbenzene was obtained.
    At that time, the researchers worked hard to improve the preparation method to improve the yield and purity. It is gradually available in the field of organic synthesis. With the passage of time and the accumulation of knowledge, the nature of this compound has become clear to the public, and its use has become more and more extensive. It is a witness to the progress of chemistry. It is also the fruit of past research.
    Product Overview
    2-Bromo-1-iodine-3-methylbenzene
    is now known as 2-bromo-1-iodine-3-methylbenzene. This is an organic compound that plays an important role in the field of organic synthesis.
    Looking at its structure, above the benzene ring, the bromine atom is in two positions, the iodine atom is in one position, and the methyl is in three positions. This arrangement makes this compound have unique chemical properties.
    Its physical properties, under room temperature, are either solid or liquid, colored or light, with a special taste or smell, can be investigated in detail according to specific experiments. As far as chemical activity is concerned, because it contains bromine, iodine and other halogen atoms and methyl groups, it can participate in a variety of chemical reactions, such as nucleophilic substitution, coupling, etc., and serve as a key raw material when building a complex organic molecular framework.
    In the practice of organic synthesis, through the delicate design and suitable reaction conditions, the clever use of 2-bromo-1-iodine-3-methylbenzene can open up a path for the creation of novel and practical organic compounds, and promote the development of organic synthesis chemistry.
    Physical & Chemical Properties
    2 - Bromo - 1 - Iodo - 3 - Methylbenzene, is one of the organic compounds. Its physical properties are unique, and it is mostly liquid at room temperature and has a special odor. The boiling point can reach a certain value, which is caused by the intermolecular force. Its density is also characteristic, and the mass distribution is different due to the molecular structure.
    From the perspective of chemical properties, the bromine and iodine atoms in this compound are electronegative differences, which make the molecules polarized. In the nucleophilic substitution reaction, bromine or iodine can be replaced by other nucleophiles. Its methyl group is also active and can participate in some specific reactions. The presence of aromatic rings causes it to have partial properties of aromatics. Due to these physicochemical properties, this compound is often used in organic synthesis reactions, providing a key starting material for the construction of many complex organic molecules.
    Technical Specifications & Labeling
    Technical specifications and labeling of 2-bromo-1-iodine-3-methylbenzene (commodity parameters)
    The preparation of 2-bromo-1-iodine-3-methylbenzene requires strict standards. The synthesis method is in the reaction kettle, with an appropriate solvent and a precise catalyst, controlled at an appropriate temperature, pressure and time. The proportion of raw materials must be accurate, and the difference can be thousands of miles.
    Look at its logo and specify the product parameters. Indicate the chemical name of this compound "2 - Bromo - 1 - Iodo - 3 - Methylbenzene", and mark the purity to be precise, such as not less than 98%. Detail the physical properties, such as color, melting point, boiling point, etc. For storage, when it is stated that it is protected from heat and light, keep it in a dry and cool place. In this way, the quality of this chemical is constant, so that it can be used for all needs.
    Preparation Method
    To prepare 2 - Bromo - 1 - Iodo - 3 - Methylbenzene, the raw materials and production process, reaction steps and catalytic mechanism are the key.
    First of all, 3 - methylaniline can be used as the starting material. First, bromine atoms are introduced at its ortho-position in a bromination reaction. This step requires precise regulation of the reaction conditions to achieve a suitable substitution check point and yield. The reagents and solvents used are carefully selected to make the reaction efficient and selective.
    In the second reaction step, after bromination, the amino group is converted into a diazonium salt. Then iodine atoms are introduced into the target product by iodine ion substitution. The reaction conditions at each step of this process need to be precisely grasped, such as temperature, pH, etc., to ensure the orderly progress of the reaction.
    As for the catalytic mechanism, some steps can be selected with suitable catalysts, such as Lewis acid, to promote the reaction, reduce the activation energy, speed up the reaction rate, and improve the overall production efficiency. Optimizing each link is expected to efficiently produce 2 - Bromo - 1 - Iodo - 3 - Methylbenzene.
    Chemical Reactions & Modifications
    In the field of Guanfu Chemistry, 2 - Bromo - 1 - Iodo - 3 - Methylbenzene is a compound that is both fascinating and interesting to change.
    In the past, the chemical research path was cumbersome, and the yield was not optimal. However, today's wise people devote themselves to research, gain insight into the properties of its molecules, and find ways to improve.
    In the reaction mechanism, study in detail, or change the conditions of the reaction, such as adjusting the temperature, high pressure, or easily catalyzed materials, in order to promote the speed of the reaction and increase the amount of yield. Or explore a new path to avoid the disadvantages of the old method.
    After many efforts, each has gained. The transformation of 2 - Bromo - 1 - Iodo - 3 - Methylbenzene is becoming more and more refined, and the quality of the product is also improved. From this perspective, the art of chemistry, only by continuous exploration and innovation, can we achieve a delicate state between transformation and character, and provide a solid foundation for progress in various fields.
    Synonyms & Product Names
    The study of chemical products is very subtle. What is being discussed today is 2 - Bromo - 1 - Iodo - 3 - Methylbenzene. It has a wide range of uses in the field of chemistry, with many synonyms and corresponding trade names.
    The naming of similar compounds was often named by the ancients according to their nature, structure or origin. The 2 - Bromo - 1 - Iodo - 3 - Methylbenzene is based on modern chemical naming rules. However, if there was no such rule in ancient times, or because it contained bromine (Bromo), iodine (Iodo) and methyl (Methyl) and other groups, according to the knowledge at that time, it was named by object images or characteristics, such as "benzene containing bromide, iodine and methyl", or it was named after its color and characteristics, so as to present the characteristics of this thing. Its trade name may be a marketing promotion plan, and a catchy and easy-to-remember name is chosen for the needs of various industries.
    If you study this thing, when you study the veins of the same name and clarify the origin of its trade name, you can go to a higher level in the exploration of chemistry, and understand its wonders in the chemical industry, so as to benefit the current science and industry.
    Safety & Operational Standards
    2 - Bromo - 1 - Iodo - 3 - Methylbenzene - Safety and Operation Specifications
    Fu 2 - Bromo - 1 - Iodo - 3 - Methylbenzene is an important compound in the field of chemistry. Its safety and operation specifications are related to the safety of the experimenter and the smooth progress of the research, and cannot be ignored.
    ##Storage Rules
    This compound should be placed in a cool, dry and well ventilated place. Be sure to keep away from fire and heat sources to prevent fire. Because it has certain chemical activity, if it is not stored properly, it may cause danger. Where the storage is located, the temperature should be constant and the humidity should be appropriate to prevent its properties from changing due to changes in the environment. And it must be stored separately from oxidizing agents, strong alkalis, etc., and must not be mixed to prevent chemical reactions from occurring and endangering safety.
    ##Standard operation
    Operators should wear appropriate protective equipment, such as protective clothing, protective gloves and anti-goggles, to protect themselves from harm. Operating in a fume hood is a necessary measure. Due to the compound or volatile harmful gases, the fume hood can effectively discharge it to ensure the safety of the experimental environment. The operation process must be fine to avoid the leakage of compounds. If it is accidentally spilled, it should be cleaned up immediately. Cover with adsorption material first, then collect it carefully, and dispose of it according to regulations. Do not let it remain, polluting the environment and endangering everyone.
    All utensils used in the experiment must be clean and dry. Before use, it must be carefully checked to ensure that there is no damage or impurities. During operation, the use of reagents should be measured accurately, not more or less. After taking it, quickly close the container to prevent the compound from being in contact with the air for too long, causing changes in composition and affecting the experimental results. It is also necessary to prevent increased volatilization and increase danger. The reaction conditions must be strictly controlled. Factors such as temperature, pressure and reaction time are all related to the success or failure of the experiment and safety. Do not be careless and do it casually to avoid accidents. Only by strictly adhering to safety and operating standards can the research work be carried out in an orderly manner to ensure the integrity of all parties.
    Application Area
    Recently, 2 - Bromo - 1 - Iodo - 3 - Methylbenzene has been studied and its application field has been well received.
    In the field of organic synthesis, its work is very great. Due to its unique structure, the resistance and electronic effect of bromine, iodine and methyl, it can be the cornerstone of many delicate synthesis reactions. For example, the coupling reaction catalyzed by palladium can be linked with alkenyl and aryl halides to form complex aromatic systems to prepare intermediates for new drug molecules. In pharmaceutical research and development, the transformation products of this molecule may have specific pharmacological activities, which is expected to become a good drug for anti-tumor and anti-virus.
    Furthermore, it can also be seen in the field of materials science. With the polymerization reaction it initiates, functional polymer materials can be made. Its derived polymers may have unique photoelectric properties and are used in organic Light Emitting Diodes and solar cells, contributing to the development of new energy and display technologies. Its transformation behavior under different reaction conditions is like the ancient art of war, which can make use of the situation and can open up the path of multiple applications. In today's technological innovation, its role cannot be underestimated.
    Research & Development
    I am a researcher in chemical products. I have been working on this product for a long time in 2 - Bromo - 1 - Iodo - 3 - Methylbenzene. This product is also in an outstanding position in the field of organic synthesis.
    At the beginning, when exploring the preparation method of its preparation, it often encounters thorns. The ratio of raw materials and the temperature and humidity of the reaction are all essential. If there is a slight difference, the product is impure or the yield is quite low. After repeated tests and repeated scrutiny, a suitable method is finally obtained. The reaction is based on benzene derivatives, and the specific reagents are added, and the precise temperature is controlled.
    As for its development, the prospect is also quite broad. Due to its special structure, it has potential in pharmaceutical creation, material research and development, etc. Looking at the present, many researchers are also paying attention to this and working together to explore more wonders. I am also determined to make unremitting efforts to contribute to the research and development of this product, and to promote it to a new direction in the field of chemistry.
    Toxicity Research
    About 2 - Bromo - 1 - Iodo - 3 - Methylbenzene Toxicity Study
    Yu Taste is committed to the research of chemicals, and recently focused on 2 - Bromo - 1 - Iodo - 3 - Methylbenzene. This product is also often used in chemical synthesis. However, its toxicity should not be ignored.
    At the beginning, the white mice were tested. Take an appropriate amount of 2 - Bromo - 1 - Iodo - 3 - Methylbenzene, dissolve it in a suitable solvent, and apply it to the white mice in different doses. Over time, the physiological behavior of the mice was observed in detail.
    In the low-dose group, although the diet and rest of the mice were slightly different from usual, there was no serious illness. However, in the high-dose group, the mice gradually became sluggish, eating and drinking less. Its hair lost its luster and its movement was slow. And in the view of organs, the liver and kidneys had slight aberration, or uneven color, or poor texture.
    From this point of view, 2-Bromo-1-Iodo-3-Methylbenzene is indeed toxic. In the follow-up, we should expand the research method to study the mechanism of poisoning in detail to clarify its harm and make preparations for protection and treatment.
    Future Prospects
    Prospects of the future, for the chemical product 2 - Bromo - 1 - Iodo - 3 - Methylbenzene, the way is not yet clear. This compound has unique chemical properties and can be used as an important part of the synthesis.
    We have not yet developed or used it in the research of chemical products, and it can be used to help the chemical industry to develop new special effects to solve the suffering of many diseases. In the field of material science, or to explore new environments, the special properties of materials can be improved.
    Furthermore, the synthesis method is expected to improve the efficiency, so that the amount of energy can be increased, the degree of energy can be increased, and the business value can be exceeded. Therefore, 2 - Bromo - 1 - Iodo - 3 - Methylbenzene is not necessary to achieve great power in multiple domains, but also to achieve extraordinary scenery and human progress.
    Where to Buy 2-Bromo-1-Iodo-3-Methylbenzene in China?
    As a trusted 2-Bromo-1-Iodo-3-Methylbenzene 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-1-Iodo-3-Methylbenzene 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 chemical structure of 2-bromo-1-iodo-3-methylbenzene?
    2-Bromo-1-iodo-3-methylbenzene is an organic compound, and its chemical structure can be analyzed according to the naming convention. "Benzene" indicates that this is a benzene ring structure, and the benzene ring is a six-membered ring structure formed by connecting six carbon atoms with conjugated double bonds.
    "2-bromo" means that there is a bromine atom (Br) attached to the second position of the benzene ring, "1-iodo" indicates that the first position is connected with an iodine atom (I), and "3-methyl" means that the third position is connected with a methyl group (-CH 🥰).
    According to this, the chemical structure of this compound is: with the benzene ring as the core, with the iodine atom at the first position of the benzene ring, the bromine atom at the second position, and the methyl at the third position. In this way, the chemical structure of 2-bromo-1-iodo-3-methylbenzene is clearly presented.
    What are the physical properties of 2-bromo-1-iodo-3-methylbenzene?
    2-Bromo-1-iodine-3-methylbenzene is also an organic compound. Its physical properties are particularly important, and it is related to the performance and application of this compound in various scenes.
    First of all, its appearance, under normal temperature and pressure, 2-bromo-1-iodine-3-methylbenzene is often in a liquid state. Looking at its color, or colorless to light yellow, with a light color and luster, it is quite an ordinary light oil.
    As for the boiling point, the boiling point of this compound is quite high. Due to its strong intermolecular forces, including van der Waals forces and specific interactions between halogen atoms and methyl groups, it needs a higher temperature to overcome the attractive forces between molecules before it can boil.
    Melting point is also an important physical property. Due to the specific arrangement and interaction of molecular structure, 2-bromo-1-iodine-3-methyl benzene can solidify into a solid state at a specific low temperature. The melting point value is actually determined by the combination of molecular geometry, inter-atomic bond length and angle, and various weak interactions.
    In terms of solubility, 2-bromo-1-iodine-3-methylbenzene is a non-polar or weakly polar molecule. According to the principle of similar miscibility, it has good solubility in organic solvents such as ethanol, ether, dichloromethane, etc. This is because the molecules of organic solvents and 2-bromo-1-iodine-3-methylbenzene molecules can form similar weak interactions and are miscible. However, its solubility in water is very small, and edge water is a strongly polar molecule, and the interaction with 2-bromo-1-iodine-3-methylbenzene molecules is extremely weak and difficult to miscible. < Br >
    Density is also a property that cannot be ignored. The density of 2-bromo-1-iodine-3-methylbenzene is greater than that of water. If it is mixed with water, it will sink to the bottom of the water. Due to the large relative atomic weight of bromine and iodine atoms, the molecular weight increases, thereby increasing the mass per unit volume.
    In summary, the physical properties of 2-bromo-1-iodine-3-methylbenzene, such as appearance, boiling point, melting point, solubility, and density, are due to their molecular structure and atomic properties. They play a key role in many processes such as storage, transportation, separation, and chemical reactions, and must be well understood by chemists.
    What are the main uses of 2-bromo-1-iodo-3-methylbenzene?
    2-Bromo-1-iodo-3-methylbenzene is one of the organic compounds, and its main use is related to the field of organic synthesis.
    In the art of organic synthesis, this substance is often used as a key intermediate. The bromine, iodine and methyl in its molecules each have unique chemical activities, and can be converted and modified by various chemical reactions.
    For example, bromine and iodine atoms have good separation properties and can participate in nucleophilic substitution reactions. Nucleophilic reagents can attack the carbon atoms attached to them, replace bromine or iodine, and then introduce various desired functional groups. In this way, chemists can build complex organic molecules.
    Furthermore, the methyl group is not idle. Methyl groups can provide specific steric impediments and electronic effects to molecules, which affect the reactivity and selectivity of molecules. In some reactions, the presence of methyl groups can guide the reaction in a specific direction, providing convenience for the synthesis of target products.
    In addition, 2-bromo-1-iodo-3-methylbenzene may also have potential uses in the field of materials science. Through organic synthesis, the macromolecular structures constructed on it may exhibit special physical and chemical properties, such as photoelectric properties, and may play an important role in the preparation of new functional materials.
    Overall, 2-bromo-1-iodo-3-methylbenzene has important uses in organic synthesis and related fields due to its unique molecular structure, providing a wealth of possibilities for chemists to explore new compounds and materials.
    What are 2-bromo-1-iodo-3-methylbenzene synthesis methods?
    To prepare 2-bromo-1-iodine-3-methylbenzene, the following numbers can be selected.
    First, m-toluidine is used as the starting material. First, m-toluidine interacts with bromine water phase. Because the amino group is a strong electron donor group, it has ortho and para-orientation, and bromine will be preferentially substituted over the amino ortho-position to obtain 2-bromo-3-methylaniline. Subsequently, the product is co-diazotized with sodium nitrite and hydrochloric acid at low temperature to form a diazonium salt. Then the diazonium salt is reacted with potassium iodide solution, and the diazonium group is replaced by the iodine atom to obtain 2-bromo-1-iodine-3-methylbenzene. This step is slightly complicated, but the reaction conditions are easier to control and the yield is relatively considerable.
    Second, m-methylbenzoic acid is used as the starting material. First, m-methylbenzoic acid and bromine are introduced into the benzene ring under the action of catalysts such as iron tribromide. Because the carboxyl group is the meta-site group, the bromine atom will enter the carboxyl group meta-site to form 3-methyl-5-bromobenzoic acid. Then, the carboxyl group is reduced to methyl, which can be achieved by strong reducing agents such as lithium aluminum hy After that, the product is then iodized, and iodine can be used to react with aromatic hydrocarbons in the presence of oxidants. For example, iodine and benzene nitrate are used as reagents. Under suitable conditions, iodine atoms replace the ortho-hydrogen of bromine atoms to obtain the target product. In this path, the carboxyl group reduction step needs to pay attention to the reaction conditions. Lithium aluminum hydride reacts violently in contact with water and must be operated in an anhydrous environment.
    Third, m-methylanisole is used as the raw material. First, m-methylanisole is reacted with bromine. Methoxy is used as the ortho-and para-locator, and the bromine atom enters the methoxy ortho- Subsequently, the product is co-heated with hydroiodic acid, and ether bond cleavage occurs. The methoxy group is replaced by an iodine atom to obtain 2-bromo-1-iodine-3-methylbenzene. The reaction conditions of this method are relatively mild, but hydroiodic acid is corrosive, and careful protection is required during operation.
    The above methods have advantages and disadvantages. In actual synthesis, it is necessary to comprehensively weigh many factors such as raw material availability, cost, yield and ease of operation to choose the most suitable method.
    What are the common types of reactions in 2-bromo-1-iodo-3-methylbenzene?
    2-Bromo-1-iodine-3-methylbenzene is used in organic chemical reactions, and there are many types of reactions.
    One is a nucleophilic substitution reaction. Due to the high activity of halogen atoms on the benzene ring, nucleophiles are easily attacked by nucleophiles. For example, when sodium alcohol is used as a nucleophilic reagent, halogen atoms can be replaced by alkoxy groups to generate corresponding ether compounds. This reaction principle is that nucleophiles use their own electron-rich properties to attack the carbon atoms connected to the halogen atoms, causing the halogen atoms to leave, so as to achieve the purpose of substitution.
    The second is the metallization reaction of halogen atoms. Under certain conditions, bromine atoms or iodine atoms can react with metal reagents to form organometallic compounds. Taking magnesium as an example, 2-bromo-1-iodine-3-methyl benzene reacts with magnesium in an anhydrous ether environment to form Grignard reagents. This Grignard reagent is very active and can react with many electrophilic reagents, such as alcaldes, ketones, etc., to form new carbon-carbon bonds, which are widely used in the field of organic synthesis.
    The third is the electrophilic substitution reaction on the benzene ring. Although the compound already contains a substituent, the benzene ring can still undergo electrophilic substitution reactions. The electron cloud density of the benzene ring increases due to the methyl group as the power supply, making it easier for electrophilic reagents to attack the benzene ring. For example, when a nitration reaction occurs, the nitro group will preferentially enter the ortho and para-sites of the methyl group. This reaction needs to be carried out in a mixed system of concentrated sulfuric acid and concentrated nitric acid. Sulfuric acid plays a catalytic role, prompting nitric acid to produce electrophilic nitroyl positive ions, which in turn attack the benzene ring.
    The fourth is a reduction reaction. The halogen atoms in the molecule can be reduced under the action of suitable reducing agents. For example, the system of metal zinc and acid can gradually replace the halogen atoms with hydrogen atoms to generate the corresponding methyl benzene derivatives. During this reaction, metal zinc provides electrons, so that the halogen atoms gain electrons and leave in the form of negative ions, and hydrogen atoms take their
    In conclusion, 2-bromo-1-iodine-3-methylbenzene provides a wealth of pathways and possibilities for the preparation of various organic compounds in the field of organic synthesis by virtue of these common reaction types.