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Benzene,4-Bromo-1-Iodo-2-(Trifluoromethyl)-

Benzene,4-Bromo-1-Iodo-2-(Trifluoromethyl)-

Hongda Chemical

    Specifications

    HS Code

    364080

    Chemical Formula C7H3BrF3I
    Molecular Weight 376.80
    Appearance Solid (predicted)
    Boiling Point 237.5°C at 760 mmHg (predicted)
    Melting Point 72 - 76 °C
    Density 2.297 g/cm³ (predicted)
    Vapor Pressure 0.0433 mmHg at 25°C (predicted)
    Logp 4.63 (predicted)
    Solubility Insoluble in water
    Flash Point 97.4°C (predicted)

    As an accredited Benzene,4-Bromo-1-Iodo-2-(Trifluoromethyl)- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 500g of 4 - bromo - 1 - iodo - 2 - (trifluoromethyl)benzene in sealed chemical - grade containers.
    Storage Store “Benzene, 4 - bromo - 1 - iodo - 2 - (trifluoromethyl)-” in a cool, dry, well - ventilated area away from heat sources and ignition sources. Keep it in a tightly - sealed container made of compatible materials, such as glass or certain plastics. Separate from oxidizing agents, reducing agents, and reactive chemicals to prevent hazardous reactions.
    Shipping Shipping of 4 - bromo - 1 - iodo - 2 - (trifluoromethyl)benzene requires compliance with hazardous chemical regulations. It should be properly packaged, labeled, and transported by carriers approved for handling such chemicals.
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    Benzene,4-Bromo-1-Iodo-2-(Trifluoromethyl)- Benzene,4-Bromo-1-Iodo-2-(Trifluoromethyl)-
    General Information
    Historical Development
    After studying the chemical substance, Benzene, 4 - Bromo - 1 - Iodo - 2 - (Trifluoromethyl) - this substance is also interesting in its historical evolution. In the past, the research of chemistry was not as detailed as it is today. At the beginning, scholars explored in the field of organic, and the knowledge of compounds containing fluorine, bromine, iodine and other halogen elements was still shallow.
    And with the advent of science and technology, the more refined the instrument, the stronger the performance of the analyte. People began to focus on such complex benzene derivatives. After many experiments, its structural characteristics were revealed. In the reaction conditions and synthesis paths, countless attempts have also been made. The yield and purity of the synthesis have been improved from the initial ignorance to the maturity of the subsequent methods. The historical evolution of this substance is really a microcosm of the development of chemistry, witnessing the unremitting research and innovation of researchers to achieve today's results.
    Product Overview
    There is a substance today called "Benzene, 4 - Bromo - 1 - Iodo - 2 - (Trifluoromethyl) -". The structure of this substance is that on the benzene ring, there are bromine atoms at four positions, iodine atoms at one position, and trifluoromethyl at two positions. Its physical properties, at room temperature, or in a specific state, and its color and taste are also characteristic. Chemical properties, due to the presence of bromine, iodine and trifluoromethyl, have different degrees of activity. Bromine and iodine atoms can participate in many nucleophilic substitution reactions, while trifluoromethyl, due to its strong electron absorption, affects the charge distribution of molecules, resulting in different chemical activities from ordinary benzene derivatives. In the field of organic synthesis, it can be a key intermediate, assist in the preparation of many complex compounds, or be used to create new materials and pharmaceuticals, with promising prospects. It is also an important substance for chemical research and industrial production.
    Physical & Chemical Properties
    4-Bromo-1-iodine-2- (trifluoromethyl) benzene, this physical property is related to chemical research. Its physical properties, at room temperature, or in a liquid state, have a specific color and odor, all of which need to be accurately inspected. The genera of its boiling point and melting point are crucial in the chemical process, separation and purification, and are related to the control of operating conditions.
    Chemical properties, due to the presence of bromine, iodine, trifluoromethyl and other functional groups, the reactivity is unique. Bromine and iodine atoms can participate in nucleophilic substitution. The strong electron-absorbing properties of trifluoromethyl affect the distribution of electron clouds in the benzene ring, resulting in different check points for electrophilic substitution reactions on the benzene ring. Or in organic synthesis, as a key intermediate, with its characteristics, to build complex organic structures and promote the industry of chemical innovation.
    Technical Specifications & Labeling
    Today there is a thing called "Benzene, 4 - Bromo - 1 - Iodo - 2 - (Trifluoromethyl) -". To clarify its technical specifications and labels (commodity parameters), it is necessary to explore in detail.
    The preparation of this substance should be based on a delicate method. The selection of raw materials must be pure, and the reaction conditions must be precisely controlled. If the temperature is controlled in a certain range, the pressure is maintained in a certain range, so that the reaction can be carried out in an orderly manner.
    As for the label, its composition and characteristics should be clearly marked. Indicate the amount of bromine, iodine and trifluoromethyl, and list the physical properties in detail, such as melting point, boiling point, etc., so that the user can understand its properties and detect its quality. In this way, this substance can be used in various applications to the fullest extent, without error, and the technical specifications and labels are clear, which is accurate for the best products.
    Preparation Method
    To prepare 4-bromo-1-iodine-2-trifluoromethyl) benzene, the raw materials and production process, reaction steps and catalytic mechanism are the key.
    The selection of raw materials needs to be cautious. Benzene derivatives containing trifluoromethyl are often used as starting materials, supplemented by brominating agents and iodizing agents. If a specific halogenated benzene is used as the base, the halogenated benzene has a substituent at a specific position in the benzene ring, which can lay the foundation for subsequent reactions.
    The first repositioning of the reaction step, with the power of the catalyst, guides the bromine atoms and iodine atoms to precisely settle in the benzene ring. For example, a transition metal catalyst is used to cleverly interact with brominating agents, iodizing agents and benzene derivatives at a suitable temperature and pressure. First bromide, followed by iodization, each step of the reaction conditions needs to be fine-tuned, such as temperature rise or fall, reaction time or delay or contraction, in order to make the reaction advance in the desired direction.
    In the catalytic mechanism, the catalyst acts like a delicate helmsman, lowering the reaction barrier and accelerating the reaction process. Transition metal catalysts use their special electronic structure to form an intermediate state with the reactants, adjusting the reaction path and making the reaction occur efficiently. In this way, 4-bromo-1-iodine-2 - (trifluoromethyl) benzene can be prepared by fine regulation of raw materials, steps and catalysis.
    Chemical Reactions & Modifications
    In the field of chemistry, there are endless changes, and the reaction and modification are wonderful, like the stars. Today there is a thing called "Benzene, 4 - Bromo - 1 - Iodo - 2 - (Trifluoromethyl) -", which has unique properties and is valued by our chemical researchers.
    Looking at its reaction, it can be changed in many ways. Or when it encounters a nucleophilic reagent, the halogen atom is translocated, and the structure is changed accordingly. The position of bromine and iodine may change differently due to the different properties and conditions of the reagents. This change is not only a structural change, but also its properties.
    The way of modification can lead others into it. With the power of chemistry, it can be combined with agents containing special functions, increase its activity, or change its physical properties. Such as adjusting its solubility and stability, making it suitable for a wider range of situations. In this way, this chemical substance can be used in materials and medicines, opening up endless possibilities for our researchers.
    Synonyms & Product Names
    A chemical substance, named "Benzene, 4 - Bromo - 1 - Iodo - 2 - (Trifluoromethyl) -", its synonym and trade name are quite worth exploring.
    In the field of chemistry, the alias of this substance may depend on its structure and properties. Looking at its structure, Bromo, iodine (Iodo) and trifluoromethyl (Trifluoromethyl) are substituted on the benzene ring, or there are people who have another alias based on this structural feature to succinctly describe its unique structure.
    As for the trade name, merchants may choose the name that is easy to remember and highlights the characteristics for the sake of promotion. It emphasizes its high purity, or highlights its special use in a certain type of reaction, so it is named.
    The existence of synonyms and trade names, although confused during communication, also reflects the diversity and wide application of chemical research from the side. Different fields and different users, based on their own needs and cognition, give them different names, enriching the culture of chemical naming.
    Safety & Operational Standards
    About 4-bromo-1-iodine-2 - (trifluoromethyl) benzene product safety and operating specifications
    Fu 4-bromo-1-iodine-2 - (trifluoromethyl) benzene is an important chemical in organic synthesis. Its unique nature is related to the safety of the experimenter and the smooth operation, so it is extremely important to set safety and operating standards.
    #1. Storage rules
    This chemical should be stored in a cool, dry and well ventilated place. Avoid open fires and hot topics, because it is sensitive to heat and is easily dangerous when heated. The storage place should be separated from oxidizing agents, strong alkalis and other substances to prevent accidents caused by interaction. The reservoir must be sealed to prevent leakage, and labeled to indicate the name, characteristics, hazards and other items.
    #2. How to use
    When taking 4-bromo-1-iodine-2 - (trifluoromethyl) benzene, the experimenter must wear protective equipment, such as experimental clothes, gloves, and goggles. Choose clean and dry equipment, and measure it accurately according to the experimental dosage. Take the measurement room, handle it with care to avoid spills and leaks. If there is a spill, dispose of it as an emergency.
    #3. The essentials of reaction operation
    Use this substance in the reaction system, and first learn the reaction mechanism and conditions. Control the temperature, pressure, reaction time and other factors, due to improper conditions or cause the reaction to run out of control. The reaction device must be well airtight and have a tail gas treatment device, because it reacts or produces harmful gases. During the operation, closely observe the reaction process, and stop abnormally quickly and check the cause.
    #4. Emergency response
    If 4-bromo-1-iodine-2 - (trifluoromethyl) benzene touches the skin, rinse with plenty of water immediately, and then wash with soap. If it enters the eye, immediately flush it with flowing water or normal saline and seek medical attention. If it is sprinkled on the ground, isolate the scene and evacuate unrelated people. Small leaks, suck with inert materials such as sand and vermiculite, and put them in a sealed container. A large amount of leaks, containment and collection, and hand it over to a professional.
    The safety and operation specifications of Fu 4-bromo-1-iodine-2 - (trifluoromethyl) benzene are the basis for the safety and success of the experiment. Experimenters must abide by it to ensure their own safety and protect the experimental environment.
    Application Area
    In the genus of benzene, there are 4-bromo-1-iodine-2 - (trifluoromethyl), which are widely used. In the field of medicine, it can make good medicines, treat all kinds of diseases, and help health recover. In the field of technology, it is a wonderful product for synthesis, increasing the nature of utensils, making them strong and beautiful. In the road of scientific research, it is the foundation of inquiry, and the assistant knows the mystery of chemistry and the change of substances. Although the derivative of benzene is small and powerful, it is related to people's livelihood and involves science and technology, its power cannot be underestimated. In today's world, science and technology are constantly evolving, and the use of this thing may be even more expanded. It is up to our generation of chemists to study it diligently to unleash its potential and create infinite benefits for the world.
    Research & Development
    Modern chemistry has flourished, and I focus on the study of compounds. Today there is a thing called "Benzene, 4 - Bromo - 1 - Iodo - 2 - (Trifluoromethyl) -", which is the object of my dedicated research.
    In order to investigate its properties and clarify its uses, I use various experimental methods to measure its physical characteristics, such as the point of melting and the state of solubility. Also explore its chemical properties, in different contexts, observe its response to other things, and study the reason for the reaction.
    After long-term research, initial results have been achieved. In specific situations, it can quickly react with a certain type of reagent to produce novel things, which may be a new way for chemical industry. However, there is still a long way to go. If you want to clarify the details, you need to collect extensive data, accumulate experience, and think about improvement strategies. I hope that in the future, I can apply this research results to industry and benefit the world, and contribute to the development of chemistry, so as to achieve my scientific ambitions.
    Toxicity Research
    One evening, Yu studied chemical products in his study, and thought of a product named "Benzene, 4 - Bromo - 1 - Iodo - 2 - (Trifluoromethyl) -". The toxicity of this product, I was worried about it, so I decided to study it.
    At first, I looked up the classics, and they all said that it was strong or harmful. Yu did not dare to be idle, so he extracted it with the ancient method, placed it in various utensils, and watched it change. Seeing that it combines with other things, the color changes and taste is different, and it is known that it is lively.
    Then, the white rat was tested and fed a small amount. During a few days, the white rat gradually withered, the diet was not good, and the fur was dull. This phenomenon shows that the poison of this thing is obvious, and it is a disaster when it enters the body.
    The more I think about it, this thing may have great uses in industry, but if its poison is not controlled, I am afraid that it will be a disaster for the common people. So I devoted myself to finding a way to reduce the harm and ensure the well-being of everyone. In the future, I can cure this poison and make the best use of it, harmless to the world.
    Future Prospects
    I have tried to study chemical products, and now looking at Benzene, 4 - Bromo - 1 - Iodo - 2 - (Trifluoromethyl) -, I feel that its future is quite promising. This compound has a unique structure, and the substitution of bromine, iodine and trifluoromethyl gives it extraordinary properties. In the field of materials science, it may become the cornerstone of new functional materials. Due to its special electronic effects, it is expected to improve the conductivity and optical properties of materials. In medicinal chemistry, it also has potential, or it can precisely act on biological targets and become specific drugs. And the balance of its stability and reactivity provides an opportunity to synthesize more complex and unique molecules. With time, in-depth exploration of its properties and reaction paths will surely lead to new applications, shining brightly in various fields, and contributing to future development.
    Where to Buy Benzene,4-Bromo-1-Iodo-2-(Trifluoromethyl)- in China?
    As a trusted Benzene,4-Bromo-1-Iodo-2-(Trifluoromethyl)- 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 Benzene,4-Bromo-1-Iodo-2-(Trifluoromethyl)- 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 Benzene, 4-Bromo-1-Iodo-2- (Trifluoromethyl) -?
    This is a question about the naming of organic compounds. According to the tradition of "Chemical Products", the naming of organic compounds follows a certain rule.
    For "Benzene, 4 - Bromo - 1 - Iodo - 2 - (Trifluoromethyl) -", the main structure is the benzene ring. Above the benzene ring, there are many substituents. "4 - Bromo" means that the 4th carbon position of the benzene ring is connected with a bromine atom; "1 - Iodo" means that the 1st carbon position is connected with an iodine atom; "2- (Trifluoromethyl) " Table 2 carbon position is connected with a trifluoromethyl.
    According to the traditional naming convention, the substituents should be listed first, and then the main structure should be described. The order in which the substituents are listed is based on their atomic number, with the smaller being the first. The atomic number of bromine (Br) is less than that of iodine (I), and trifluoromethyl (-CF) also has its specific order.
    Therefore, the Chinese name of this compound is: 4-bromo-1-iodine-2 - (trifluoromethyl) benzene. This naming not only conforms to the rules passed down in "Chemical Engineering", but also accurately shows the structural characteristics of the compound, so that industry insiders can know its approximate structure after hearing its name, which is of great significance in chemical research and practice.
    What are the physical properties of Benzene, 4-Bromo-1-Iodo-2- (Trifluoromethyl) -?
    4-Bromo-1-iodine-2- (trifluoromethyl) benzene, this is an organic compound. Depending on its physical properties, it is usually liquid at room temperature and pressure, but the specific state may change due to surrounding environmental factors. Its color is nearly colorless, or slightly yellowish, and the transparency is quite high.
    Regarding the melting point, due to its intermolecular forces and structural characteristics, the melting point is about -20 ° C, and the boiling point is roughly in the range of 180-190 ° C. The lower melting point is due to the introduction of trifluoromethyl, bromine and iodine atoms into the molecular structure, which results in relatively weakened intermolecular forces, making it easier to convert from solid to liquid; the higher boiling point is due to the increase in molecular mass and the enhancement of intermolecular van der Waals forces by halogen atoms.
    Its density is greater than that of water, about 2.1-2.3g/cm ³. If placed in water, it will sink to the bottom. In terms of solubility, it has little solubility in polar solvents such as water. Due to its strong non-polar molecular structure, the polarity difference with water is significant, and it follows the principle of "similar miscibility". However, in common organic solvents, such as ether, chloroform, dichloromethane, and other non-polar or weakly polar solvents, the solubility is quite good, and it can be well miscible with them.
    In addition, the compound is volatile and will slowly evaporate in the air, emitting a special odor. And because it contains halogen atoms and trifluoromethyl, it has different chemical stability. Under specific conditions, it can participate in a variety of chemical reactions and exhibit unique chemical properties.
    What are the chemical properties of Benzene, 4-Bromo-1-Iodo-2- (Trifluoromethyl) -?
    This is 4-bromo-1-iodine-2 - (trifluoromethyl) benzene, which has the general characteristics of aromatics in terms of chemical properties.
    From the perspective of electrophilic substitution reaction, the electron cloud density of the benzene ring has a significant effect. Because trifluoromethyl is a strong electron-absorbing group, it will reduce the electron cloud density of the benzene ring, and the electrophilic substitution reaction activity is lower than that of benzene. And this group reduces the electron cloud density of the ortho-and para-site of the benzene ring more than the meta-site, so the electrophilic substitution reaction mainly occurs in the meta-site. For example, during nitrification, the nitro group mainly enters the meta-site to obtain the meta-substitution product.
    In terms of the characteristics of halogen atoms, although bromine and iodine are ortho and para-localizers, the electron cloud density of the benzene ring can increase in the ortho and para-localizers, and the electrophilic substitution reaction activity of the benzene ring can be enhanced. However, due to the combined effect of steric hindrance and electronic effect, the localization effect may be slightly deviated from the theory in some reactions.
    In terms of oxidation reaction, the compound is more difficult to be oxidized. Due to the strong electron absorption of trifluoromethyl, the benzene ring structure is stabilized, making it difficult to be oxidized by common oxidants. However, under certain harsh conditions, such as high temperature and strong oxidants, the benzene ring may be destroyed.
    In addition, the halogen atoms it contains can participate in nucle Under appropriate nucleophilic reagents and reaction conditions, bromine or iodine atoms can be replaced by nucleophilic reagents to form corresponding replacement products. In this process, the tendency of halogen atom departure is related to the activity of halogen atoms. Usually, iodine atoms are more likely to leave than bromine atoms, because the bond energy of C-I bond is less than that of C-Br bond.
    What is the main use of Benzene, 4-Bromo-1-Iodo-2- (Trifluoromethyl) -?
    4-Bromo-1-iodine-2- (trifluoromethyl) benzene is an organic compound. It has a wide range of uses and is a key intermediate in the field of organic synthesis.
    In the field of medicinal chemistry, it can be used to construct complex molecular structures with specific physiological activities. For example, its side chains can be connected to active functional groups through a series of organic reactions, thus creating new drug molecules and providing more possibilities for drug development.
    In the field of materials science, it also plays an important role. With its unique chemical structure and properties, it can be used to prepare special functional materials. Such as fluoropolymer materials, which can improve the chemical stability, weather resistance and surface properties of materials. After rational design and reaction, it can become the structural unit of the polymer, endowing the material with unique properties and meeting the requirements of material properties in different application scenarios.
    Furthermore, in the preparation of fine chemical products, 4-bromo-1-iodine-2 - (trifluoromethyl) benzene can be used as a starting material to synthesize high-value-added fine chemicals through multi-step reactions, such as special fragrances, pigments, etc., to meet the market demand for high-quality fine chemical products.
    Overall, although 4-bromo-1-iodine-2- (trifluoromethyl) benzene is an organic compound, it plays an indispensable role in many fields such as medicine, materials, and fine chemicals, promoting the sustainable development and innovation of related fields.
    What are the preparation methods of Benzene, 4-Bromo-1-Iodo-2- (Trifluoromethyl) -
    There are various ways to prepare 4-bromo-1-iodine-2- (trifluoromethyl) benzene.
    First, it can be started from a suitable aromatic hydrocarbon substrate. Based on aromatic hydrocarbons containing trifluoromethyl, bromine atoms are introduced first. This can be achieved by interacting with brominating reagents under appropriate reaction conditions. If liquid bromine is used as a bromine source, under the catalysis of Lewis acids (such as iron tribromide), aromatics can undergo electrophilic substitution reactions to introduce bromine atoms at specific positions in aromatic rings. This step requires attention to the reaction temperature and reagent ratio to prevent the formation of polybrominated products.
    Next, iodine atoms are introduced. A halogen atom exchange reaction can be used to react with a suitable iodine substitution reagent (such as potassium iodide, etc.) in a specific organic solvent (such as N, N-dimethylformamide, etc.) under heating conditions. In this process, the halogen atom is substituted, so that the iodine atom is connected to the aromatic ring, thereby obtaining 4-bromo-1-iodine-2 - (trifluoromethyl) benzene.
    Second, it can also be used to gradually build an aromatic ring. First prepare an intermediate containing trifluoromethyl and bromine atoms, and then introduce iodine atoms at the same time through a suitable cyclization reaction. If an unsaturated compound containing trifluoromethyl and bromine atoms is used as a raw material, an iodine source is added to the reaction system through cyclization reaction, and an aromatic ring structure is constructed through multi-step reaction. At the same time, the layout of bromine, iodine and trifluoromethyl based on the specific position of the benzene ring is achieved.
    To prepare this compound, an appropriate method is selected according to various factors such as the availability of raw materials, the ease of control of reaction conditions and cost, so as to achieve the purpose of efficient and economical synthesis.