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What are the main uses of 1-Bromo-3-Chloro-5- (Trifluoromethyl) Benzene?
1-Bromo-3-chloro-5- (trifluoromethyl) benzene is also an organic compound. It has a wide range of uses and is often used as a key intermediate in the field of organic synthesis.
First, in the preparation of medicinal chemistry, specific functional groups can be introduced through a series of reactions to construct biologically active molecular structures, thus laying the foundation for the creation of new drugs. In the process of many drug development, such halogenated and trifluoromethyl benzene derivatives can endow drugs with unique physicochemical properties and biological activities, such as improving the lipid solubility of drugs and enhancing their affinity with targets, etc., helping to develop new drugs with high efficiency and low toxicity.
Second, in the field of materials science, this compound can be used as a raw material to prepare materials with special functions. Such as the preparation of fluoropolymer materials, the introduction of trifluoromethyl can significantly improve the chemical stability, weather resistance, low surface energy and other characteristics of the material. Such materials are widely used in coatings, plastics, fibers and other industries, which can improve the quality and performance of materials to meet the needs of different scenarios.
Third, in the field of pesticide chemistry, it also has important functions. By means of organic synthesis, it is converted into pesticide ingredients with insecticidal, bactericidal or herbicidal activities. The structure of halogen and trifluoromethyl helps to enhance the effect of pesticides on target organisms, while reducing the impact on the environment, in line with the development trend of modern green pesticides.
In short, 1-bromo-3-chloro-5- (trifluoromethyl) benzene plays an important role in promoting technological progress and innovative development in various fields.
What are the physical properties of 1-Bromo-3-Chloro-5- (Trifluoromethyl) Benzene?
1-Bromo-3-chloro-5- (trifluoromethyl) benzene is also an organic compound. Its physical properties are particularly important, and it is related to its performance in various chemical processes and practical applications.
First of all, on its phase and appearance, under normal temperature and pressure, it is mostly a colorless to light yellow liquid. Due to the arrangement and interaction of atoms in the molecular structure, it has such appearance characteristics. Its light color also suggests the characteristics of intramolecular electron transitions and other effects.
Second, its melting point and boiling point. The melting point is about -30 ° C, and the boiling point is in the range of 190-192 ° C. The melting point is low, and the intermolecular force is not extremely strong, making it difficult to closely arrange the molecules into a solid state at relatively low temperatures. If the boiling point is high, the intermolecular force is enhanced due to the atoms or groups such as bromine, chlorine and trifluoromethyl in the molecule, and higher energy is required to vaporize it.
Furthermore, the density of this compound is greater than that of water, about 1.7 g/cm ³. Due to the presence of heavy atoms such as bromine and chlorine in the molecule, the mass per unit volume is increased. And because it is an organic substance, it is insoluble with water. This is because water is a polar molecule, while 1-bromo-3-chloro-5- (trifluoromethyl) benzene has a weaker polarity. According to the principle of "similar miscibility", the two are difficult to miscible.
Its volatility is moderate. Although it is not very volatile, it can still evaporate slowly into the air under appropriate temperature and environment. And it has a certain smell, but it is difficult to describe the smell accurately. It is often said that it has a special smell similar to halogenated aromatics. The generation of this smell is due to the joint action of halogen atoms and benzene rings in the molecular structure.
In addition, the compound has good solubility in organic solvents, such as ether, dichloromethane, tetrahydrofuran and other common organic solvents. Due to the similar intermolecular forces between organic solvents and the compound, it can be mixed with each other. This property is very beneficial to the reaction and the separation of products when used in organic synthesis and other fields.
What are the synthesis methods of 1-Bromo-3-Chloro-5- (Trifluoromethyl) Benzene?
The synthesis method of 1-bromo-3-chloro-5- (trifluoromethyl) benzene covers a variety of paths. First, it can be started from aryl halides. Bromine, chlorine and trifluoromethyl groups are introduced by a suitable halogenated aromatic hydrocarbon through a specific nucleophilic substitution reaction. If a chlorinated aromatic hydrocarbon is used as the starting material, under appropriate conditions, it is reacted with a brominating agent to introduce bromine atoms. This bromination reaction requires the selection of a suitable catalyst and reaction solvent, and the reaction temperature and time are controlled to achieve good selectivity and yield.
Then, through a special method, trifluoromethyl is introduced into the benzene ring. Trifluoromethylation reagents can be used to replace the hydrogen on the benzene ring with trifluoromethyl in a specific reaction system. This step requires strict reaction conditions and requires precise regulation of reaction parameters to ensure the smooth progress of the reaction and high product purity.
Second, it can also be constructed from derivatives of the benzene ring. For example, benzene derivatives containing appropriate substituents are used as substrates, and the target group is gradually introduced through multi-step reactions. First, chlorine atoms are introduced at specific positions in the benzene ring through a suitable reaction, and then bromine atoms and trifluoromethyl atoms are introduced in sequence. In this process, each step of the reaction needs to be carefully planned, taking into account the influence of each substituent on subsequent reactions, in order to avoid unnecessary side reactions.
Third, the reaction strategy of metal catalysis can also be used. With the help of the unique activity and selectivity of metal catalysts, halogenation and trifluoromethylation at specific positions on the benzene ring are achieved. For example, metal catalysts such as palladium and copper are used to couple the substrate with the corresponding reagent under the synergistic action of ligands to construct the target compound. This method requires optimizing the type and dosage of metal catalysts and ligands to improve the reaction efficiency and product yield.
All these synthesis methods have their own advantages and disadvantages, and it is necessary to carefully choose the appropriate method according to the actual situation, such as the availability of raw materials, cost considerations, product purity requirements, etc., in order to achieve the purpose of efficient synthesis of 1-bromo-3-chloro-5- (trifluoromethyl) benzene.
What are the precautions for storing and transporting 1-Bromo-3-Chloro-5- (Trifluoromethyl) Benzene?
1-Bromo-3-chloro-5- (trifluoromethyl) benzene is an organic chemical substance, and many matters need to be paid careful attention during storage and transportation.
First storage, because of its certain chemical activity, must be stored in a cool, dry and well-ventilated place. Excessive temperature can easily cause chemical reactions, and humid environment or cause its hydrolysis and other accidents, so it is crucial to maintain a dry environment. And it is necessary to keep away from fire and heat sources. Many of these compounds are flammable or can cause dangerous reactions when heated. If they are close to the fire source, they may cause fire or even explosion.
Furthermore, they should be stored separately from oxidizing agents, strong bases and other substances. 1-Bromo-3-chloro-5- (trifluoromethyl) benzene can react violently with oxidizing agents, and strong bases may also cause changes in its molecular structure, causing it to deteriorate or produce dangerous products. The storage place should be clearly marked, indicating its name, nature and emergency treatment methods, so that personnel can know that if something happens, appropriate measures can be taken quickly.
As for transportation, relevant regulations on the transportation of hazardous chemicals should be followed. The transportation container must be strong and well sealed to prevent leakage. The selected container material should not chemically react with the compound to ensure stability during transportation. The transportation vehicle should also be equipped with necessary emergency equipment, such as fire extinguishers, leakage emergency treatment tools, etc.
Transportation personnel must be professionally trained and familiar with the chemical's characteristics and emergency response methods. During transportation, close attention should be paid to temperature, pressure and other conditions to avoid violent vibration and impact, so as to prevent package damage and cause 1-bromo-3-chloro-5 - (trifluoromethyl) benzene to leak, endangering the environment and personal safety. In this way, the safety of 1-bromo-3-chloro-5 - (trifluoromethyl) benzene during storage and transportation must be ensured.
What are the safety risks associated with 1-Bromo-3-Chloro-5- (Trifluoromethyl) Benzene?
1-Bromo-3-chloro-5- (trifluoromethyl) benzene related safety risks are as follows:
Fire and explosion risk
This compound is an organic halogen, although it is not flammable by itself, but in case of open fire and hot topic, the hydrocarbon part of its molecular structure can participate in the combustion reaction. If burned, halogen atoms will generate irritating gases such as hydrogen halide. And in high temperature environments, it may decompose and release toxic fumes containing fluorine, chlorine and bromine. These fumes are not only harmful to the human body, but may also react with substances in the surrounding environment in a complex manner, increasing the difficulty of fire fighting. Improper storage, such as contact with strong oxidants, may trigger a violent redox reaction, resulting in combustion or even explosion.
Health Hazard Risk
1. ** Inhalation Hazard **: Inhalation of its volatile vapor can irritate the respiratory mucosa, causing symptoms such as cough, asthma, shortness of breath, etc. Long-term or large-scale inhalation may damage lung tissue, affect gas exchange function, and in severe cases can lead to chemical pneumonia or even pulmonary edema. Among them, trifluoromethyl groups have strong biological activity, which may interfere with normal physiological and metabolic processes after entering the human body, and damage the nervous system and endocrine system.
2. ** Skin Contact Hazard **: Contact with skin can cause irritation, causing skin redness, itching, and pain. Since the compound contains halogen atoms, halogen atoms can react with biological macromolecules such as proteins in the skin, destroying the normal structure and function of the skin. In severe cases, it may cause skin burns, ulcers, and if not treated in time, it may also cause infection.
3. ** Eye Contact Hazards **: Accidentally splashed into the eyes, it will strongly irritate the conjunctiva and cornea, causing severe eye pain, tears, redness and swelling, and may even damage vision. If not treated in time, it may cause permanent eye damage.
4. ** Hazards of accidental ingestion **: After ingestion, it will cause serious corrosion to the oral cavity, throat, esophagus and gastrointestinal mucosa, causing nausea, vomiting, abdominal pain, diarrhea and other symptoms. After entering the human circulatory system, it will be distributed to various organs and tissues of the body with blood, further damaging the function of important organs such as liver and kidney.
Risk of environmental hazards
1. ** In soil **: It has certain chemical stability and is difficult to be rapidly degraded by microorganisms in the soil. It may remain in the soil for a long time, affecting the ecological structure and function of the soil, inhibiting the growth and reproduction of beneficial microorganisms in the soil, which in turn affects the absorption of nutrients by plant roots, resulting in plant growth inhibition or even death.
2. ** In water **: It will pollute the water source and be toxic to aquatic organisms. The halogen atom and trifluoromethyl group contained in it can interfere with the physiological and biochemical processes of aquatic organisms, affect the growth, reproduction and survival of fish and plankton, and destroy the balance of aquatic ecosystems. And it may accumulate in high trophic organisms through bioaccumulation in the food chain, eventually posing a potential threat to human health.