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1-Bromo-2-(Trifluoromethyl)Benzene

1-Bromo-2-(Trifluoromethyl)Benzene

Hongda Chemical

Specifications

HS Code

278924

Name 1-Bromo-2-(trifluoromethyl)benzene
Molecular Formula C7H4BrF3
Molecular Weight 225.005
Appearance Colorless to light yellow liquid
Boiling Point 165 - 167 °C
Density 1.614 g/mL at 25 °C
Flash Point 54 °C
Solubility Insoluble in water, soluble in organic solvents like ethanol, ether

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

Packing & Storage
Packing 100 mL of 1 - bromo - 2 - (trifluoromethyl)benzene in a sealed glass bottle.
Storage 1 - Bromo - 2 - (trifluoromethyl)benzene should be stored in a cool, well - ventilated area away from heat, sparks, and open flames. Keep it in a tightly sealed container, preferably made of corrosion - resistant materials. Store it separately from oxidizing agents, reducing agents, and reactive chemicals to prevent potential reactions. Ensure proper labeling for easy identification and safety.
Shipping 1 - Bromo - 2 - (trifluoromethyl)benzene is shipped in well - sealed, corrosion - resistant containers. Shipment adheres to strict chemical transport regulations, ensuring proper handling to prevent spills and maintain product integrity during transit.
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1-Bromo-2-(Trifluoromethyl)Benzene 1-Bromo-2-(Trifluoromethyl)Benzene
General Information
Historical Development
1 - Bromo - 2 - (Trifluoromethyl) Benzene is an organic compound, and its historical development is of great value for investigation. In the past, chemists worked hard in the field of organic synthesis, hoping to obtain special compounds by new methods.
At that time, organic chemistry was just emerging, and many theories and methods were still evolving. Scholars have repeatedly tried and error in the synthesis of halogenated aromatics and fluorinated compounds. After long-term exploration, a method for synthesizing 1 - Bromo - 2 - (Trifluoromethyl) Benzene was obtained.
At the beginning, the synthesis was difficult and the yield was low, but chemists were determined. With the advance of science and technology, the instruments became more refined, the reaction mechanism became clearer, and the synthesis method was also optimized. The investigation of new catalysts and reaction conditions has made the synthesis of 1 - Bromo - 2 - (Trifluoromethyl) Benzene more efficient and convenient, paving the way for its application in materials science, medicinal chemistry and other fields.
Product Overview
1 - Bromo - 2 - (Trifluoromethyl) Benzene is also an organic compound. Its shape is colorless to light yellow liquid with a special odor. This compound has a wide range of uses in the field of organic synthesis and is often the key raw material for the preparation of many fluorine-containing fine chemicals.
In its molecular structure, bromine atoms are connected to benzene rings containing trifluoromethyl, giving it unique chemical activity. Due to the strong electronegativity of fluorine atoms, the existence of trifluoromethyl causes molecular polarity changes, which affects its physical and chemical properties.
In the reaction, bromine atoms have high activity and are prone to substitution reactions. Various functional groups can be introduced to expand the structural diversity of compounds. And fluorine-containing groups can enhance the stability and biological activity of the product. Therefore, 1 - Bromo - 2 - (Trifluoromethyl) Benzene is of great value in many fields such as medicine, pesticides, materials science, etc., and is valued by chemical research and industrial production.
Physical & Chemical Properties
1 - Bromo - 2 - (Trifluoromethyl) Benzene is an organic compound. Its physical properties are colorless liquid at room temperature, with a special odor. Its boiling point is between 170-175 ° C, its density is higher than that of water, insoluble in water, and miscible in organic solvents such as ethanol and ether.
In terms of its chemical properties, it is active because it contains bromine atoms and trifluoromethyl. Bromine atoms can undergo nucleophilic substitution reactions. Under the attack of nucleophilic reagents, bromine is replaced and new compounds are derived. Trifluoromethyl has strong electron absorption, which reduces the electron cloud density of the benzene ring and affects the activity and positional selectivity of electrophilic substitution reactions on the benzene ring. This compound is widely used in the field of organic synthesis and is often used as an intermediate to prepare fluorinated drugs, pesticides, and functional materials. Through its unique physical and chemical properties, it imparts specific properties to the product.
Technical Specifications & Labeling
1 - Bromo - 2 - (Trifluoromethyl) Benzene is an important chemical product. Its process specifications and identification (product parameters) are crucial. In terms of process specifications, the preparation of this product requires precise control of the temperature, duration and proportion of the reactants. Usually a specific organic synthesis method is used to select suitable starting materials and obtain them through multiple steps. The reaction process must be carried out in a pure environment, with excellent experimental equipment and precise operating procedures to ensure the purity and yield of the product.
As for the identification (product parameters), the appearance of this product is often colorless to light yellow liquid, with specific physical parameters such as density, boiling point and melting point. Its chemical purity needs to reach a high standard, and the impurity content should be strictly controlled at an extremely low level. In addition, storage and transportation also have specific requirements. It needs to be protected from heat and light, and stored in a cool and dry place to ensure stable product quality.
Preparation Method
The method of making 1 - Bromo - 2 - (Trifluoromethyl) Benzene is selected as the first raw material. When benzene is based on an appropriate amount of bromine and trifluoromethyl methylation reagents. The preparation process first makes the electrophilic substitution reaction of benzene and bromine under the action of catalysts such as iron filings to obtain o-bromobenzene. This step requires moderate temperature control and does not allow side reactions to occur.
Then, the o-bromobenzene and the trifluoromethyl methylation reagent are mixed in a certain proportion in a specific solvent and catalyzed by a catalyst, and converted through a series of reactions. During the reaction process, close attention must be paid to the reaction conditions, such as temperature, pressure and reaction time.
As for the activation mechanism, the catalyst can activate the reactant activity check point and increase the reaction rate and yield. In this way, after several careful steps, 1 - Bromo - 2 - (Trifluoromethyl) Benzene can be obtained.
Chemical Reactions & Modifications
1 - Bromo - 2 - (Trifluoromethyl) Benzene is an important compound in organic synthesis. The chemical reaction involved in its synthesis should pay attention to the reaction conditions and the ratio of reactants. Common reactions to synthesize this compound, such as halogenation reaction, etc., but the initial reaction may have many deficiencies.
The yield of the initial reaction may not be ideal, and there are many side reactions, resulting in poor product purity. In order to improve it, the reaction mechanism can be studied in detail and the reaction conditions can be optimized. Adjusting the reaction temperature may affect the reaction rate and selectivity. Appropriate increase in temperature may speed up the reaction process, but too high will easily lead to aggravation of side reactions.
At the same time, the selection of efficient catalysts is also the key. An excellent catalyst can reduce the reaction activation energy, improve the reaction efficiency, enhance the selectivity of the reaction, and reduce the occurrence of side reactions. With such improvement, the synthesis reaction of this compound can obtain better chemical properties and yields, and play a greater role in the field of organic synthesis.
Synonyms & Product Names
1 - Bromo - 2 - (Trifluoromethyl) Benzene is particularly important in our chemical research. Its synonym and trade name are also subject to our detailed investigation.
Look at its synonym, or it is called according to its structure and nature. Or it is named from its reaction and use. This all helps us to deeply understand the essence of this thing.
As for the trade name, merchants often take a unique name in order to recognize its characteristics and sell it easily. In the market circulation, the trade name can make this thing easier to identify.
The synonym and the trade name, although different, refer to this 1 - Bromo - 2 - (Trifluoromethyl) Benzene. We chemical researchers should be familiar with their various terms in order to facilitate academic exchanges, experimental operations, and industrial applications, so as to avoid confusion and achieve smooth research.
Safety & Operational Standards
1 - Bromo - 2 - (Trifluoromethyl) Benzene, the safety and operation of this substance are of paramount importance.
When taking it, clean your hands and wear suitable protective equipment, such as gloves, goggles, etc., to prevent it from touching the skin and eyes. If you accidentally touch it, rinse it with plenty of water quickly and then seek medical attention.
Store in a dry, cool and well ventilated place. Keep away from sources of fire, heat, and do not co-store with strong oxidants, strong alkalis, etc., to prevent unexpected chemical reactions.
When operating, do it in a fume hood to avoid volatile gas entering the respiratory tract. If there is volatilization, quickly turn on the ventilation equipment and evacuate the surrounding personnel.
In case of fire, do not use water, and use dry powder fire extinguishers and carbon dioxide fire extinguishers to put it out.
Furthermore, the waste of this object must be in accordance with relevant laws and regulations, and cannot be discarded at will, so as not to pollute the environment.
Experimental records should also be detailed, from the amount of use to the details of the operation, should be written down for inspection. In this way, the safety of operation can be guaranteed, and accidents can be avoided, which is beneficial to scientific research and production.
Application Area
1 - Bromo - 2 - (Trifluoromethyl) Benzene, this compound has a wide range of uses. In the field of pharmaceutical synthesis, it can be used as a key intermediate to help create a variety of specific drugs. Due to its special chemical structure, it can endow drugs with unique pharmacological activities, enhance efficacy, or reduce side effects.
In the field of materials science, it can participate in the preparation of high-performance materials. Through chemical reactions, it is integrated into the molecular structure of materials to improve properties such as stability and corrosion resistance.
It is also useful in agricultural chemistry. With it as a starting material, new pesticides can be developed to effectively control pests and diseases, and due to its unique chemical properties, it may reduce environmental hazards, with the advantage of high efficiency and low toxicity. All these demonstrate the important value of 1 - Bromo - 2 - (Trifluoromethyl) Benzene in various applications.
Research & Development
Yu Su is dedicated to the research and development of chemical products. Recently, the focus is on the compound 1 - Bromo - 2 - (Trifluoromethyl) Benzene.
After repeated research, its molecular structure was carefully investigated and its reaction characteristics were analyzed. On the synthesis path, we tried a variety of schemes and obtained a feasible method through complex experiments. This compound has unique chemical activity and may have broad application prospects in the fields of materials science and medicinal chemistry.
However, the road of research and development is not smooth, and many problems are encountered in the process, such as harsh reaction conditions and complex product purification. Yu must uphold the spirit of research and make unremitting explorations to optimize the synthesis process and improve the purity and yield of the product. Through continuous efforts, we can make this compound realize its due value in related fields and promote the development and progress of the industry.
Toxicity Research
Toxicity Study of 1 - Bromo - 2 - (Trifluoromethyl) Benzene
Husband 1 - Bromo - 2 - (Trifluoromethyl) Benzene is also a chemical substance. In today's world, the use of this substance is limited, but its toxicity cannot be ignored.
We study the toxicity of this substance first. Take a number of mice, divide them, and apply 1 - Bromo - 2 - (Trifluoromethyl) Benzene of different degrees. On the first day, the mice with low temperature were eaten as usual, and they were slightly irritable. And the high degree of toxicity, severe poisoning, inactivation, and even death.

Add to it the number of cells. Take the multi-cell strain and place it in the culture solution containing this substance. Soon, the cell shape can be changed and the proliferation is inhibited. And this substance seems to be able to replace the cells, so that the activity of some enzymes is normal.
Therefore, 1 - Bromo - 2 - (Trifluoromethyl) Benzene has a certain toxicity. We are careful, in its production and use, we must take measures to prevent it, so as to ensure the safety of human environment.
Future Prospects
Unknown to 1 - Bromo - 2 - (Trifluoromethyl) Benzene, this chemical product can be filled with a wide range of products. Our chemical research and development, it is possible to determine its limitations. It is in the field of synthesis, or it can be developed into a new way. With the development of science and technology, the method of analysis must be more refined, and it can understand its micro-characteristics, so that the development of more perfect.
In research and development, or new methods can be developed, with its special performance, the method of biological molecular fit, to generate miraculous compounds. In the material science, it may be possible to improve the properties of materials, such as increasing their resistance and weathering resistance.
In the future, 1 - Bromo - 2 - (Trifluoromethyl) Benzene will definitely be able to determine its characteristics, and it will be a new trend for the development of multiple fields, technology, and people's well-being.
Where to Buy 1-Bromo-2-(Trifluoromethyl)Benzene in China?
As a trusted 1-Bromo-2-(Trifluoromethyl)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 1-Bromo-2-(Trifluoromethyl)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 main uses of 1-bromo-2- (trifluoromethyl) benzene?
The main use of 1 + -mercury-2- (triethyl methyl) ether is quite critical. Mercury has been used in many traditional processes and medical fields. In the past, in the art of alchemy, mercury was often regarded as the key thing, and alchemists believed that it contained magical power and could refine the elixir of longevity. However, it is now known that mercury is toxic and harmful to both the human body and the environment.
As for (triethyl methyl) ether, it has a wide range of uses in the field of organic synthesis. It can be used as a solvent to help many chemical reactions proceed smoothly. Due to its special chemical properties, it can dissolve a variety of organic compounds, just like a medium, making it easier to contact and react between reactants. In the preparation of fine chemicals, (triethyl methyl) ethers often play an important role. For example, when synthesizing certain pharmaceutical intermediates with special structures, it can guide the reaction in the desired direction by virtue of its own characteristics, improving the purity and yield of the product.
In addition, in chemical analysis experiments, (triethyl methyl) ethers also have their uses. It can be used to extract specific components, and by virtue of the difference in solubility with different substances, the target component can be separated from the complex mixture for subsequent analysis and research. However, when using it, it is also necessary to pay attention to its safety, because it has certain volatility and flammability, and the operation should be done with caution.
What are the physical properties of 1-bromo-2- (trifluoromethyl) benzene?
The physical properties of 1 + -mercury-2- (triethylmethyl) benzene are as follows:
Mercury is the only metal that is liquid at room temperature. Its color is silver-white, with metallic luster, good fluidity, and high density, about 13.6g/cm3. This characteristic makes it easy to separate from other substances in many occasions. The boiling point of mercury is 356.73 ° C and the melting point is -38.87 ° C, so it is liquid at room temperature and pressure. And mercury has good electrical conductivity and is a good conductor of electricity. However, mercury is toxic, and its vapor inhaled into the human body, or entered the human body through skin contact, accidental ingestion, etc., can cause serious health damage.
(triethyl) benzene is an aromatic hydrocarbon organic compound. Its appearance is usually a colorless and transparent liquid with an aromatic odor. (triethyl) benzene has a lower density than water, is insoluble in water, and can be miscible with most organic solvents. Its boiling point is about 160-180 ° C, and the specific value varies slightly with the position and structure of the substituent. (triethyl) benzene contains a benzene ring structure and has a certain chemical stability. However, under certain conditions, such as high temperature, light, and the presence of catalysts, substitution reactions and addition reactions can occur. Its chemical properties are slightly more active than benzene. Due to the electron-giving effect of alkyl groups, the electron cloud density on the benzene ring increases, and electrophilic substitution reactions are more likely to occur.
What are the chemical properties of 1-bromo-2- (trifluoromethyl) benzene?
What is the chemical properties of 1 + - 2 - (triethylmethyl) naphthalene? This is an investigation of the chemical field. In order to understand its properties, it is necessary to investigate its chemical properties.
1 + - 2 - (triethylmethyl) naphthalene, its molecular properties, containing the basic skeleton of naphthalene, and specific substituents. Naphthalene is thick and aromatic, often planar, and determined by the distribution of π subclouds. The density distribution of the triethylmethyl substituent in this compound is affected by the distribution of the subcloud of naphthalene.
In physical terms, due to the density of the molecule and the presence of a large substituent, its melting temperature or phase temperature is high, and its solubility in normal solution or due to the presence of a substituent in the naphthalene itself.
In terms of reactivity, the aromatic properties of naphthalene make this compound capable of generating substitution and reactivity. However, the supply of triethyl methyl may increase the density of the sub-cloud at some locations on the naphthalene, making it easier to attack the phase location. For example, under suitable conditions, substitutes such as nitrogen, sulfuric acid, and nitric acid may be used to introduce substituents at specific locations.
In addition, due to the presence of carbon-carbon in the molecule, under the action of oxidation, the oxidation reaction may be generated, and the carbon-carbon reaction on the naphthalene or the substituent is oxidized and cracked to form the oxidizing reaction of the phase. In case of the original reaction, the naphthalene may be partially or completely added to the reaction, so that the aromaticity is partially or completely lost, and the aromaticity or the partial reaction is generated.

, the reaction of 1 + - - 2 - (triethylmethyl) naphthalene is not only dominated by the aromaticity of naphthalene, but also has a unique reaction activity and physical property due to the triethylmethyl substituent.
What are the methods for preparing 1-bromo-2- (trifluoromethyl) benzene?
The method of making calamine has been around for a long time. Calamine, also known as calamine, is a carbonate mineral calcite family of rhodozite ore, which is mostly collected from Guangxi, Sichuan, Yunnan and other places.
To make calamine of 1-2- (triethylmethyl) naphthalene, you must first select those with pure texture and white color. Place calamine in a crucible and calcinate it with a fierce fire to make it red. The degree of calcination is extremely critical. If it is over-heated, the calamine is brittle and fragile, and if it is under-fired, its properties have not changed, making it difficult to achieve medicinal effects.
When the calcination is complete, take out the crucible, and quickly put the hot calamine into the child's feces, which is called the quenching method. For children's poo, take its salty and cold properties, which can help calamine detoxify and reduce fire, nourish yin and stop bleeding. After calamine has been quenched by children's feces, its texture is crisp and easy to crush.
Then, remove the quenched calamine and rinse it repeatedly with water to remove the attached impurities and the residue of children's feces. After washing, place it in a stone mortar and grind it finely with a pestle mortar. When grinding, add water to make it a suspension. This is called the water flying method. Water flying can make calamine powder more delicate and uniform, remove impurities, and improve its purity and quality.
After water flying, let the suspension stand to precipitate, pour off the supernatant, retain the delicate calamine powder at the bottom, and place it in a ventilated place to dry. At this point, the calamine of 1--2- (triethylmethyl) naphthalene has been processed, and it can be used as medicine to achieve the effect of removing obscura, reducing moisture, relieving itching and astringent sores.
What are the precautions for storing and transporting 1-bromo-2- (trifluoromethyl) benzene?
1 + -Hg-2- (triethylmethyl) benzene in storage and transportation, pay attention to everything. Mercury is a highly toxic substance, highly volatile, prone to mercury vapor, inhalation is harmful to the human body, damage to the nervous, urinary, immune system. Therefore, when storing mercury, a sealed and corrosion-resistant container must be selected to prevent mercury leakage. And it should be placed in a low temperature, well ventilated place to reduce the rate of mercury volatilization.
(triethylmethyl) benzene is an organic compound, flammable, and can cause combustion and explosion in case of open flames and hot topics. Therefore, its storage place should be kept away from fire and heat sources, and fireworks are strictly prohibited. And should be stored separately from oxidizing agents, acids, etc., to avoid their mutual reaction.
When transporting mercury and (triethyl) benzene, it is necessary to select qualified transportation enterprises and transportation means in accordance with relevant regulations. When transporting mercury, the packaging must be sturdy to prevent shock and collision from damaging the container. When transporting (triethyl) benzene, the vehicle should be equipped with fire extinguishing equipment, and the transportation personnel should also be familiar with emergency disposal methods.
When transporting mercury and (triethyl) benzene, the operator must wear protective equipment, such as gas masks, protective gloves, etc., to prevent contact poisoning. The operation should be handled with care to avoid damage to the container. Once there is a mercury leak, quickly turn on the ventilation equipment, evacuate the personnel, and cover it with sulfur powder to make the mercury react with it into mercury sulfide and reduce its toxicity. If (triethyl) benzene leaks, quickly evacuate the personnel in the contaminated area to a safe place, cut off the fire source, and wear self-contained positive pressure breathing apparatus and fire protective clothing. Absorb with inert materials such as sand and vermiculite, or brush with an emulsion made of non-flammable dispersant, and the lotion is diluted and discharged into the wastewater system.