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4-Bromo-3,5-Dichloro-1-(Trifluoromethoxy)Benzene

4-Bromo-3,5-Dichloro-1-(Trifluoromethoxy)Benzene

Hongda Chemical

    Specifications

    HS Code

    707837

    Chemical Formula C7H2BrCl2F3O
    Molecular Weight 307.90
    Appearance Typically a colorless to pale - yellow liquid or solid
    Boiling Point Data may vary, around a certain temperature depending on purity
    Melting Point Specific melting point value based on purity
    Density A certain value in g/cm³
    Solubility In Water Low solubility in water
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
    Vapor Pressure A particular value at a given temperature
    Flash Point A specific temperature indicating flammability risk

    As an accredited 4-Bromo-3,5-Dichloro-1-(Trifluoromethoxy)Benzene 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 - 3,5 - dichloro - 1 - (trifluoromethoxy)benzene in sealed chemical - grade containers.
    Storage 4 - bromo - 3,5 - dichloro - 1 - (trifluoromethoxy)benzene should be stored in a cool, dry, well - ventilated area, away from heat sources and open flames. Keep it in a tightly - sealed container, preferably made of corrosion - resistant materials like glass. Store it separately from oxidizing agents, reducing agents, and other reactive chemicals to prevent potential reactions.
    Shipping 4 - bromo - 3,5 - dichloro - 1 - (trifluoromethoxy)benzene is shipped in well - sealed, corrosion - resistant containers. Shipment follows strict chemical transportation regulations to ensure safe transit, avoiding exposure to heat, moisture, and incompatible substances.
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    4-Bromo-3,5-Dichloro-1-(Trifluoromethoxy)Benzene 4-Bromo-3,5-Dichloro-1-(Trifluoromethoxy)Benzene
    General Information
    Historical Development
    4 - Bromo - 3,5 - Dichloro - 1 - (Trifluoromethoxy) Benzene The evolution of chemical substances
    is really related to the rise of science and technology. 4 - Bromo - 3,5 - Dichloro - 1 - (Trifluoromethoxy) Benzene This compound, at the beginning of its birth, was only hidden in the secluded realm of academic research. At that time, scholars worked tirelessly in the laboratory to explore its synthesis method. At the beginning, the synthesis path was full of thorns, low yield, and impurities.
    However, the years pass, and technology is changing. Chemists study the principle, improve the process, and use innovative methods to gradually solve the problem of synthesis. The clever selection of catalysts and the precise control of reaction conditions are all key. After several years of research, the yield has gradually increased and the quality has been improved. From the prototype of the laboratory to the scale of industrial production, this compound has gradually emerged in the chemical field, and the scope of application has gradually expanded. It has injected new energy into the development of many industries, which is a bright page in the history of chemical substances.
    Product Overview
    4-Bromo-3,5-dichloro-1- (trifluoromethoxy) benzene is also an organic compound. Its form may be a colorless liquid with a specific odor.
    In this compound, bromine, chlorine, and trifluoromethoxy groups endow it with unique chemical properties. Bromine atoms are active and often act as leaving groups in nucleophilic substitution reactions, promoting the progress of the reaction. Chlorine atoms are electron-absorbing, which affects the electron cloud distribution of molecules, reducing the electron cloud density of benzene rings, and causing the reaction activity to change during electrophilic substitution reactions. Trifluoromethoxy groups are characterized by strong electron absorption and good stability, which significantly affect the physical and chemical properties of compounds.
    It is widely used in the field of organic synthesis and can be used as a key intermediate to prepare various organic materials with special functions, pharmaceuticals and pesticides. In the field of fine chemistry, it is also an important synthetic building block, assisting researchers in constructing complex organic molecular structures.
    Physical & Chemical Properties
    The physicochemical properties of 4-bromo-3,5-dichloro-1- (trifluoromethoxy) benzene are particularly important. Looking at its properties, at room temperature, it is either a colorless to light yellow liquid, or a crystal, with a special odor. Its melting point and boiling point are the key elements to characterize the physical properties. The melting point is in a specific range, giving it the characteristics of phase change at the corresponding temperature. The boiling point is also fixed, revealing the energy required for its conversion from liquid to gaseous state.
    Discussing chemical properties, the presence of bromine, chlorine and trifluoromethoxy in this compound gives it unique reactivity. Bromine and chlorine atoms can participate in nucleophilic substitution reactions, providing the possibility for the introduction of other functional groups under appropriate conditions. The strong electron-absorbing properties of trifluoromethoxy group affect the electron cloud density distribution of benzene ring, which then affects its chemical behavior. In many organic synthesis reactions, it shows different reaction paths and products. These physicochemical properties are of great significance in chemical production, drug research and development and other fields.
    Technical Specifications & Labeling
    4 - Bromo - 3,5 - Dichloro - 1 - (Trifluoromethoxy) Benzene is also a product of transformation. The quality of the product (the quality of the product) is very important. The quality of the technology of this thing is important. It is clear how it is made, how it is made, and how it is refined. Its quality, its name, and its form make it known. And in the quality of the product, such as melting, boiling, density, etc., can not be ignored. This is all because of its quality and its characteristics. In ancient words, if you want to make this thing, you must follow the quality, its raw materials, and control its quality, so that you can get a good product. In addition, it can be used to demonstrate its general characteristics, which is clear to users at a glance, and it is essential to meet the requirements of the technical standard (commodity quality).
    Preparation Method
    The raw material of 4 - Bromo - 3,5 - Dichloro - 1 - (Trifluoromethoxy) Benzene is the key to the production process, reaction steps and catalytic mechanism.
    First take an appropriate amount of 3,5 - dichlorophenol as the starting material, add an appropriate amount of potassium carbonate as the acid binding agent in the reaction kettle, and use N, N - dimethylformamide as the solvent. Stir well. Warm up to a suitable temperature, slowly add trifluoromethoxy bromide dropwise, control the dripping speed, and make the reaction proceed smoothly. This reaction step requires close attention to the temperature and reaction time to prevent side reactions.
    After the reaction is completed, the product is extracted with an organic solvent, washed with water, dried and other processes to remove impurities. After that, it is distilled under reduced pressure to obtain a crude product. Then refined by column chromatography to obtain 4 - Bromo - 3,5 - Dichloro - 1 - (Trifluoromethoxy) Benzene with high purity. The whole process, the catalytic mechanism is effective in improving the reaction rate and improving the purity of the product, which is crucial to success and failure.
    Chemical Reactions & Modifications
    Fu 4 - Bromo - 3,5 - Dichloro - 1 - (Trifluoromethoxy) Benzene, in the field of chemistry, its reaction and modification are of great importance to scholars. Looking at its structure, the halogen atom is combined with a special oxygen group, which is the end of the reactivity.
    Its reaction, or nucleophilic substitution, can be easily replaced by its halogen atom, and when it encounters a nucleophilic reagent, the halogen is easily replaced by another group. If it encounters an alkoxide salt, the halogen atom leaves, and the alkoxy group enters to form a new ether.
    As for modification, or adjusting its electrical properties, introducing a power supply or a power-absorbing group, changing its reactivity and selectivity. Or increasing the chain of the benzene ring, expanding its structure, and expanding its application. After this reaction and modification, it can be used to produce special drugs or functional materials, which can be used in medicine and materials industries.
    Synonyms & Product Names
    Today there is a thing called 4 - Bromo - 3,5 - Dichloro - 1 - (Trifluoromethoxy) Benzene. This is a chemical substance that is often used in various studies.
    The alias and trade name of this thing are also our investigation. The alias is derived because of its characteristics, structure or previous names, and the trade name is related to market circulation and identification. In the academic world, there are different names or different names, but they all refer to this thing.
    If we explore its many names, we can better understand its application in different situations, and also help to unify and expand knowledge. Looking at the process of chemical research in the past, it was quite common to have more than one thing. The reason for this is that there are different regions or different uses, so the names are different. Today, a detailed study of the aliases and trade names of 4 - Bromo - 3,5 - Dichloro - 1 - (Trifluoromethoxy) Benzene is an indispensable part of chemical research.
    Safety & Operational Standards
    4 - Bromo - 3,5 - Dichloro - 1 - (Trifluoromethoxy) Benzene Safety and Operation Specifications
    Fu 4 - Bromo - 3,5 - Dichloro - 1 - (Trifluoromethoxy) Benzene is an important substance in chemical research. Its experimental operation and storage are subject to strict safety and operation standards, which cannot be ignored.
    This substance has certain chemical activity. When operating, the experimenter must wear appropriate protective equipment. Protective clothing is required to avoid contact with the skin and prevent the risk of chemical burns. And when wearing protective gloves, the material must be resistant to corrosion to ensure hand safety. Facial protection is also essential. Protective glasses can prevent it from splashing into the eyes and avoid eye damage.
    Ventilation of the experimental environment is essential. When this substance is placed in a well-ventilated laboratory bench, the volatile gas can be quickly discharged to prevent it from accumulating in the air, so as to prevent respiratory diseases or other health problems.
    For storage, 4-Bromo-3,5-Dichloro-1- (Trifluoromethoxy) Benzene should be stored in a cool, dry and ventilated place. Keep away from fire and heat sources, because it may be flammable or easily decomposed by heat, causing safety accidents. And it must be stored separately from oxidizing agents and reducing agents to prevent mutual reaction.
    There are also rules for the operation process. When taking it, use clean and suitable utensils to measure it accurately to avoid waste and pollution. If there is any spill, clean it up immediately and deal with it in accordance with relevant regulations. Do not let it remain.
    Furthermore, the experimenter must be familiar with emergency response methods. If it comes into contact with the skin, rinse it with plenty of water immediately, followed by an appropriate antidote. If it splashes into the eyes, immediately open the eyelids, rinse with running water or normal saline, and seek medical attention immediately.
    In short, in the research and use of 4 - Bromo - 3,5 - Dichloro - 1 - (Trifluoromethoxy) Benzene, strict safety and operating standards are adhered to to to ensure the safety of the experiment and the smooth research.
    Application Area
    4-Bromo-3,5-dichloro-1- (trifluoromethoxy) benzene is used in many fields. In the field of medicinal chemistry, it is a key intermediate. With exquisite organic synthesis technology, special anti-disease drugs can be prepared to help health. In the field of materials science, special treatment can give materials unique properties, such as enhancing their corrosion and wear resistance, for the manufacture of high-end equipment parts. In the field of agricultural chemistry, it may be reasonably formulated to make high-efficiency and low-toxicity pesticides to protect crops from pests and insect infestation. All of these demonstrate its important value in the application field, which cannot be ignored in chemical research and industrial production.
    Research & Development
    In recent years, in the field of chemistry, 4 - Bromo - 3,5 - Dichloro - 1 - (Trifluoromethoxy) Benzene has gradually become the focus of our chemical researchers. Its structure is unique and its properties are different, and it has considerable potential in various fields of organic synthesis.
    We study this compound in detail to explore its synthesis method. At the beginning, we tried various paths and encountered many obstacles. The choice of raw materials and the method of reaction need to be carefully considered. After repeated tests, we finally obtained a better method, which can increase its yield and maintain its purity.
    At the end of the application, this compound can be used as an intermediate to participate in various organic reactions. The products derived from it can be used in the field of medicine or materials.
    We should continue to study, optimize the synthesis technology, and expand the application path, so that 4 - Bromo - 3, 5 - Dichloro - 1 - (Trifluoromethoxy) Benzene can contribute more to the advancement of chemistry and industry. In this way, we can live up to our researchers' responsibilities and promote the vigorous development of this field.
    Toxicity Research
    Today, there is a product named 4 - Bromo - 3,5 - Dichloro - 1 - (Trifluoromethoxy) Benzene. I am a chemist to investigate its toxicity. The structure of this product is unique, and groups such as bromine, chlorine, and trifluoromethoxy are combined in the benzene ring. The investigation of its toxicity is related to the safety of life and environmental changes.
    The study of human toxicity, the first thing to look at is its response to biomolecules. Or intersect with proteins, nucleic acids, etc., and disrupt its physiological order. In cells, or when the membrane is broken, it disrupts the metabolic process. Test it in animals to detect its symptoms, such as abnormal behavior and organ damage. And considering its dispersion in the environment, water, soil, and air can all exist, or accumulate the biological chain, resulting in ecological imbalance.
    Those of us who transform, should be careful and careful, study the toxicity of this thing in detail, for the safety of the world and the health of the living beings, and do our best to make sure its nature is clear to prevent it from suffering.
    Future Prospects
    Fu 4 - Bromo - 3,5 - Dichloro - 1 - (Trifluoromethoxy) Benzene is also a chemical product. Looking at its structure, bromine, chlorine, and trifluoromethoxy are connected in an orderly manner, and have unique chemical properties.
    In the future, this product may emerge in the field of medicine. Because of its special structure, it can be used as a key intermediate to help create new drugs to solve difficult diseases. In materials science, it may be the cornerstone of new functional materials, making materials specific for photoelectricity, thermal conductivity, etc.
    To achieve this vision, researchers need to work together. Optimize the synthesis method, reduce costs and increase productivity; explore the performance in detail, and clarify its mechanism of action. In this way, the potential of this product can be fully developed, and it will bloom in the fields of future science and technology and people's livelihood, and contribute to human well-being.
    Where to Buy 4-Bromo-3,5-Dichloro-1-(Trifluoromethoxy)Benzene in China?
    As a trusted 4-Bromo-3,5-Dichloro-1-(Trifluoromethoxy)Benzene 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 4-Bromo-3,5-Dichloro-1-(Trifluoromethoxy)Benzene 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 chemical properties of 4-Bromo-3,5-Dichloro-1- (Trifluoromethoxy) Benzene?
    4-Bromo-3,5-dichloro-1- (trifluoromethoxy) benzene, this is an organic compound. Its chemical properties are unique and worthy of in-depth investigation.
    From the structural point of view, on the benzene ring of the compound, bromine atoms, dichloro atoms and trifluoromethoxy atoms are in their respective positions. These substituents have a profound impact on its chemical properties.
    First of all, its physical properties are usually colorless to light yellow liquids or solids. Due to the force between molecules, the melting boiling point is affected by the type and location of the substituent. Its relative density also has a specific value due to the molecular composition.
    In terms of chemical properties, the conjugate system of the benzene ring makes it stable to a certain extent. However, the presence of the substituent gives it a different reactivity. Bromine atoms can participate in nucleophilic substitution reactions, and bromine atoms can be replaced by other nucleophilic groups under suitable reagents and conditions. Dichlorine atoms can also participate in similar reactions under specific circumstances. Due to the difference in electronegativity, the electron cloud density distribution of the benzene ring changes, which affects the reaction check point and activity.
    Trifluoromethoxy, with the strong electron absorption of trifluoromethyl, makes the electron cloud of the benzene ring more biased towards this group, so that the density of the adjacent and para-position electron clouds on the benzene ring is relatively reduced, and the meta-position is relatively increased, which in turn affects the localization effect of the electrophilic substitution reaction. This compound may be used as an intermediate in organic synthesis to prepare complex organic molecules with specific biological activities or material properties. The reaction in which it participates often requires fine regulation of factors such as the proportion of reactants, temperature, and catalyst according to the desired product and reaction conditions to achieve the ideal reaction effect and product purity.
    What are the main uses of 4-Bromo-3,5-Dichloro-1- (Trifluoromethoxy) Benzene?
    4-Bromo-3,5-dichloro-1- (trifluoromethoxy) benzene has a wide range of uses. In the field of organic synthesis, it is often used as a key intermediate. The technique of covering organic synthesis aims to construct complex organic molecules. This compound can introduce specific functional groups through various chemical reactions, such as nucleophilic substitution and coupling reactions, and then synthesize many organic compounds with special structures and properties.
    In the field of materials science, it is also of great value. Materials research and development seeks substances with unique properties. Such benzene compounds may be used as raw materials and processed by specific processes to prepare materials with special electrical, optical or thermal properties. For example, in the preparation of optoelectronic materials, its structural properties may endow the material with excellent charge transport ability, thereby improving the photoelectric conversion efficiency.
    In the field of pharmaceutical chemistry, there is also no shortage of its presence. Drug development requires the search for molecular structures with specific biological activities, the special structure of 4-bromo-3,5-dichloro-1- (trifluoromethoxy) benzene, or make it potentially biologically active. On this basis, after chemical modification and optimization, new drugs are expected to be developed for the treatment of various diseases.
    In addition, in the field of pesticide chemistry, there is also the possibility of application. The creation of pesticides requires compounds that are effective in killing pests, pathogens and environmentally friendly. The structural characteristics of this compound may make it have certain biological activity, which can be used as a starting material for pesticide research and development. After further research and improvement, high-efficiency and low-toxicity pesticide products can be developed to escort agricultural production.
    In summary, 4-bromo-3,5-dichloro-1- (trifluoromethoxy) benzene plays an important role in many fields such as organic synthesis, materials science, medicine and pesticide chemistry, and is an organic compound with a wide range of uses.
    What is the synthesis method of 4-Bromo-3,5-Dichloro-1- (Trifluoromethoxy) Benzene?
    The method for synthesizing 4-bromo-3,5-dichloro-1- (trifluoromethoxy) benzene can follow the following steps.
    The first step is to use an appropriate starting material, such as a halogenated benzene derivative, which needs to have a suitable substituent for subsequent introduction of trifluoromethoxy. In this case, a benzene ring compound with bromine and chlorine atoms can be selected, and its position should be in line with the position of the bromine and chlorine atoms in the target product.
    The second step is to introduce a trifluoromethoxy group. The common method is to use a trifluoromethylation reagent, such as trifluoromethyl halide or trifluoromethylsulfonate. Under suitable reaction conditions, such as in the presence of a base, the base can help the substrate form a nucleophilic species, and then undergo nucleophilic substitution reaction with the trifluoromethoxy reagent. The choice of base is crucial. Common bases include inorganic bases such as potassium carbonate and sodium carbonate, or strong organic bases such as potassium tert-butyl alcohol, which need to be carefully selected according to the characteristics of the substrate and reaction conditions. The reaction temperature also needs to be precisely controlled, usually under moderate heating conditions, such as 50-100 ° C. The specific temperature depends on the reaction process and the substrate activity.
    Furthermore, during the reaction process, the choice of solvent should not be underestimated. Appropriate solvents can enhance the solubility of the substrate and the reagent and promote the reaction. Common aprotic solvents, such as N, N-dimethylformamide (DMF), dimethyl sulfoxide (DMSO), etc., are often preferred because of their stabilizing effect on ionic reaction intermediates.
    After the reaction is completed, the product needs to be separated and purified. This can be achieved by various means, such as column chromatography, using silica gel as the stationary phase, selecting an appropriate eluent, and separating the product and impurities according to the difference in the partition coefficient between the stationary phase and the mobile phase. Or use the recrystallization method to select a suitable solvent to dissolve the product in a hot solvent, crystallize and precipitate after cooling, and the impurities remain in the mother solution to obtain a pure 4-bromo-3,5-dichloro-1 - (trifluoromethoxy) benzene product.
    What are the precautions for 4-Bromo-3,5-Dichloro-1- (Trifluoromethoxy) Benzene during storage and transportation?
    4-Bromo-3,5-dichloro-1- (trifluoromethoxy) benzene is also an organic compound. During storage and transportation, many matters must be paid attention to.
    Storage is first mentioned. This compound may be more active in nature, and it should be placed in a cool and dry place. It may deteriorate due to adverse reactions such as hydrolysis due to moisture. And a cool place can reduce the risk of reaction due to excessive temperature. The storage place should be away from fire and heat sources, both of which can warm the compound and promote uncontrollable chemical changes. Furthermore, it should be stored separately from oxidizing agents and reducing agents. This compound may have a certain redox activity, coexisting with oxidizing agents and reducing agents, it is easy to cause violent reactions, and even the risk of explosion. The storage place also needs to be equipped with suitable materials to contain leaks, in case of leakage, it can be dealt with in time.
    As for transportation, it should not be underestimated. The transportation vehicle must ensure that the vehicle is in good condition, and the shock-proof and collision-proof facilities are complete. Leakage is caused by bumps or collisions on the road, or the container containing the compound is broken. During transportation, temperature and humidity must be strictly controlled to maintain a suitable environment. And the transportation personnel should be familiar with the characteristics of the compound and emergency treatment methods. In case of emergencies, they can respond quickly and properly. In addition, the vehicle containing this item must not be mixed with other contraband items to avoid interaction and cause disaster. In this way, it is necessary to ensure the safety of 4-bromo-3,5-dichloro-1 - (trifluoromethoxy) benzene during storage and transportation without causing accidental changes.
    What are the effects of 4-Bromo-3,5-Dichloro-1- (Trifluoromethoxy) Benzene on the environment and human health?
    4-Bromo-3,5-dichloro-1- (trifluoromethoxy) benzene is of great concern to the world about its impact on the environment and human health.
    If this substance is scattered in the environment, it is stable, difficult to decompose, or causes long-term accumulation in water and soil. In aquatic environments, it may harm various organisms such as fish, shrimp, shellfish and algae, disturb their growth and reproduction order, and even cause population changes. In terrestrial domains, it may be absorbed by plants, disrupt their physiological functions, or pass through the food chain, causing enrichment in high-end organisms and endangering ecological balance.
    As for the human body, if ingested through breathing, diet or skin contact, it may be a serious disaster. It may damage the nervous system of the human body, causing trance, memory loss, and slow movement. In the immune system, or make it dysfunctional, causing the human body to be susceptible to diseases. The reproductive system is also difficult to escape, or cause fertility problems, such as fetal malformations and infertility. And this substance may pose a risk of cancer. Long-term exposure may increase the risk of cancer.
    Although the research on its chemical properties and similar substances is not complete at present, the potential threat to the environment and human health should not be underestimated. Everyone should treat it with caution, and scientific researchers also need to investigate it diligently to clarify its harm, find ways to prevent and resolve it, and protect the tranquility of the environment and the health of the human body.