Chemical Formula | C7H4ClF3 |
Molar Mass | 180.554 g/mol |
Appearance | Colorless to light yellow liquid |
Odor | Pungent odor |
Boiling Point | 139 - 141 °C |
Melting Point | -48 °C |
Density | 1.326 g/cm³ at 20 °C |
Solubility In Water | Insoluble |
Vapor Pressure | 1.94 kPa at 25 °C |
Flash Point | 38 °C |
Refractive Index | 1.443 (20 °C) |
What are the main uses of M-Chlorobenzotrifluoride?
M-Chlorobenzotrifluoride, or m-chlorotrifluorotoluene, has a wide range of main uses and is widely used in various fields of chemical industry.
In the process of pharmaceutical synthesis, this is an important starting material and intermediate. The preparation process of many drugs relies on it as a basis to build a specific molecular structure. For example, the synthesis of some compounds with specific pharmacological activities can introduce key functional groups through their unique chemical properties, thereby shaping the active parts of drug molecules, so that the finished drug can play a role in specific physiological targets, and help the research and development of medicine to move towards precision and efficiency.
In the process of pesticide creation, m-chlorotrifluorotoluene is also a key element. The pesticide made from it has excellent insecticidal, bactericidal and herbicidal effects. Due to its stable chemical structure and specific lipophilicity, it can effectively penetrate the body surface of pests or the stratum corneum of plants, enrich and exert medicinal effect at the check point, providing a strong guarantee for the control of pests and diseases in agricultural production, and improving crop yield and quality.
Furthermore, in the field of materials science, it can be used to synthesize special polymer materials. Such as the preparation of engineering plastics with excellent heat resistance and chemical corrosion resistance, such materials are indispensable in high-end fields such as aerospace and electronics. The polymerization reaction participated by m-chlorotrifluorotoluene can endow polymer materials with unique properties and meet the strict requirements of materials in extreme environments.
In the dye industry, m-chlorotrifluorotoluene also has a place. It can be used to synthesize new dyes with bright colors, light resistance and washable properties. Its structural properties make the dye molecules more firmly bonded to fibers and other substrates, and endow the dyes with unique optical properties. It broadens the application scope of dyes and meets the needs of high-quality dyes in textile, printing and dyeing industries.
In summary, m-chlorotrifluorotoluene is an important chemical raw material in many fields such as medicine, pesticides, materials, and dyes due to its unique chemical structure and properties. It promotes technological innovation and development in various industries.
What are the physical properties of M-Chlorobenzotrifluoride?
The physical properties of M-chlorotrifluorotoluene are as follows:
This substance is mostly a colorless and transparent liquid at room temperature. Looking at its appearance, it is clear and free of impurities. Its odor is slightly irritating, and it has a special smell.
When it comes to the boiling point, it is about 139-141 ° C. At this temperature, the liquid will turn into a gaseous state and rise. The melting point is very low, about -57.7 ° C. When the temperature drops to this point, the liquid that originally flowed will condense into a solid state.
Its density is about 1.378g/cm ³, which is heavier than water. If it is placed in one place with water, it will sink at the bottom of the water.
M-chlorotrifluorotoluene is insoluble in water, and the two meet, such as oil and water, which are distinct and incompatible with each other. However, it has good solubility in organic solvents, such as benzene and toluene of aromatic hydrocarbons, trichloromethane and dichloroethane of halogenated hydrocarbons, etc., and can be miscible with it into a uniform phase.
Its vapor pressure has a corresponding value at a specific temperature, which is related to its difficulty of volatilization. The higher the vapor pressure, the easier it is to volatilize under the same conditions.
And because of the characteristics of its molecular structure, the substance has a certain stability. Under normal environmental conditions, it is not easy to chemically react and deteriorate. However, in case of extreme conditions such as hot topics and open flames, there are also potential dangers.
What is the chemistry of M-Chlorobenzotrifluoride?
M-Chlorobenzotrifluoride, m-chlorotrifluorotoluene, is an organic compound with unique chemical properties. Its properties are stable, but under certain conditions, it can also show a lively side.
From the perspective of physical properties, this is a colorless to light yellow liquid with a pungent odor. Its boiling point is about 139-141 ° C, and its density is 1.37 g/mL. It is insoluble in water, but it can be miscible with most organic solvents, such as ethanol, ether, benzene, etc. This solubility makes it often used as a solvent in organic synthesis reactions, providing a homogeneous environment for the reaction, helping the reactants to fully contact and accelerate the reaction process.
In terms of chemical properties, although the chlorine atoms on the benzene ring have certain stability, they can still participate in the nucleophilic substitution reaction. Due to the strong electron-absorbing effect of trifluoromethyl, the electron cloud density of the benzene ring decreases and the activity of chlorine atoms increases. For example, under the action of strong bases and specific catalysts, chlorine atoms can be replaced by hydroxyl, amino and other nucleophilic reagents to form corresponding meta-substitution products, which lays the foundation for the synthesis of various fluorine-containing organic compounds.
Furthermore, trifluoromethyl is a strong electron-absorbing group, which significantly affects the distribution of the electron cloud of the benzene ring. This not only reduces the activity of the electrophilic substitution reaction of the benzene ring, but also affects the localization effect of the In electrophilic substitution reactions, new substituents tend to enter the meta-site, which is crucial in the design of organic synthesis routes, which can help chemists to precisely prepare meta-substituted fluoroaromatic hydrocarbon derivatives.
In addition, M-Chlorobenzotrifluoride can also participate in some oxidation and reduction reactions involving benzene rings to generate organic compounds with different structures and functions. It is widely used in the fields of medicine, pesticides, materials, etc., and can be used as a key intermediate for the synthesis of new drug molecules, high-efficiency pesticides and high-performance fluorine-containing materials.
What is the preparation method of M-Chlorobenzotrifluoride?
The method of preparing M-chlorotrifluorotoluene is obtained by the two-step reaction of chlorination and fluorination with m-chlorotoluene as the starting material.
First take m-chlorotoluene, place it in a chlorination kettle, add an appropriate amount of catalyst, such as azobisisobutyronitrile, and pass chlorine gas. At a suitable temperature, about 100-120 ° C, stir the reaction. In this chlorination process, the hydrogen atom on the methyl group of m-chlorotoluene is gradually replaced by the chlorine atom to produce m-chlorotrichlorotoluene. The reaction is quite critical, and the temperature and the rate of chlorine gas introduction need to be strictly controlled. If the temperature is too high, it is easy to cause side reactions to increase, and the product is not pure; if the rate is too fast, it is difficult to make the reaction
After the chlorination reaction is completed, transfer the obtained m-chlorotoluene to a fluorination kettle. Add a fluorinating agent, such as anhydrous hydrogen fluoride, or potassium fluoride. The reaction is carried out under a certain pressure, about 2-3 MPa, and a temperature of 150-180 ° C. This fluorination step aims to replace the chlorine atom on the methyl group in m-chlorotoluene with a fluorine atom to obtain M-chlorotrifluorotoluene. In the fluorination reaction, the amount of fluorinating agent and the reaction time affect the yield and purity of the product. Excessive fluorinating agent may promote the complete reaction, but it also increases the cost; if the time is insufficient, the product will not be fully converted. < Br >
At the end of the reaction, the unreacted raw materials, by-products and impurities are removed by distillation, extraction and other separation and purification methods to obtain pure M-chlorotrifluorotoluene. This preparation method, although the steps are slightly complicated, but through fine control of the reaction conditions, high-purity target products can be obtained to meet the needs of industry and scientific research.
M-Chlorobenzotrifluoride what are the precautions during use
M-chlorotrifluorotoluene is a commonly used raw material in organic synthesis. When using it, many things must be paid attention to.
Bear the brunt, safety protection is the top priority. This substance is irritating, or harmful to the eyes, skin and respiratory tract. During operation, appropriate protective equipment must be worn, such as protective glasses, gloves and gas masks, to avoid direct contact and inhalation.
Second, storage conditions cannot be ignored. It should be stored in a cool, well-ventilated place, away from fire, heat sources, and stored separately from oxidants and alkalis to avoid dangerous reactions.
Furthermore, during use, precisely control the dosage, and carefully measure and add according to the reaction needs to prevent excessive adverse consequences. The operating environment needs to be well ventilated to drain volatile gaseous substances in time.
In addition, it is flammable, and open flames and hot topics must be prohibited around it. Use explosion-proof ventilation systems and equipment to prevent combustion and explosion caused by open flames or hot topics.
If you accidentally contact, emergency treatment should not be delayed. If you contact the skin, rinse with a large amount of flowing water immediately; if you contact the eyes, lift the eyelids, rinse with flowing water or normal saline, and then seek medical attention. Inhalers, quickly leave the scene to fresh air, keep the respiratory tract unobstructed, if breathing difficulties, oxygen, breathing stop, immediately perform artificial respiration and seek medical attention.
Proficient operation is also the key. Operators must be specially trained, strictly abide by the operating procedures, and must not act blindly.
All of these are important items that should be paid attention to when using M-chlorotrifluorotoluene. Only careful operation and comprehensive protection can ensure that the security is safe and the synthesis is smooth.