2 Chloro 4 Fluorobenzyl Cyanide
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
2-Chloro-4-fluorobenzyl cyanide
Chemical Formula C8H5ClFN
Molar Mass 169.58 g/mol
Appearance Colorless to light yellow liquid
Boiling Point Around 257 - 258 °C
Density Approx. 1.26 g/cm³
Solubility In Water Poorly soluble
Solubility In Organic Solvents Soluble in common organic solvents
Vapor Pressure Low vapor pressure at room temperature
Odor May have a characteristic, pungent odor
Chemical Formula C8H5ClFN
FAQ

What are the main uses of 2-Chloro-4-fluorobenzyl cyanide?

2-Chloro-4-fluorobenzyl cyanide has a wide range of uses. In the field of pharmaceutical synthesis, it is often a key intermediate. Due to its unique molecular structure, it can build a complex drug molecular structure through specific chemical reactions. For example, when developing some antibacterial and antiviral drugs, it can be used as a starting material to introduce key functional groups through multi-step reactions, and finally synthesize drugs with specific pharmacological activities.

It also has important value in the creation of pesticides. Many high-efficiency and low-toxicity pesticide varieties can be derived. For example, it can design and synthesize herbicides and insecticides that target specific pests or weeds. Due to its structural characteristics, it can precisely act on target organisms, interfere with their physiological activities, achieve good control effects, and have little impact on the environment and non-target organisms.

In addition, in the field of materials science, it may also have potential uses. It can participate in the preparation of special polymer materials, endowing materials with unique properties, such as improving heat resistance, chemical corrosion resistance, etc. By polymerizing with other monomers, its structural units are introduced into the polymer chain, thereby improving the comprehensive properties of materials and meeting the needs of different industrial scenarios.

In summary, 2-chloro-4-fluorobenzyl cyanide has significant uses in the fields of medicine, pesticides and materials, providing important basic raw materials for the development of related industries.

2-Chloro-4-fluorobenzyl the physical properties of cyanide

2-Chloro-4-fluorobenzyl cyanide, this is an organic compound. Its physical properties are unique and related to many fields such as chemical industry and medicine.

When it comes to appearance, under normal temperature and pressure, 2-chloro-4-fluorobenzyl cyanide is often colorless to light yellow liquid, with clear texture and clear visual perception. This color property is easy to observe and distinguish in practical applications. In the relevant production process, its purity and state can be preliminarily judged by its appearance to ensure stable production.

Boiling point is one of the important physical parameters of substances. The boiling point of 2-chloro-4-fluorobenzyl cyanide is in a specific range, about [X] ° C. Knowing the boiling point is of great significance. In chemical operations such as distillation and separation, the temperature can be precisely controlled according to the difference in boiling point to achieve effective separation of the substance from other components, achieve the purpose of purification, and then improve product quality.

In terms of melting point, the melting point of 2-chloro-4-fluorobenzyl cyanide is [X] ° C. The characteristics of the melting point have a profound impact on the storage and transportation of substances. For example, when transporting or storing in a low temperature environment, the melting point should be considered to prevent the substance from solidifying, causing the container to break or inconvenient subsequent use.

Solubility is also a key property. 2-Chloro-4-fluorobenzyl cyanide is insoluble in water, but soluble in organic solvents such as ethanol, ether, acetone, etc. This solubility characteristic plays a significant role in organic synthesis reactions. When using it as a raw material or intermediate, the appropriate organic solvent can be selected according to the solubility to create a suitable reaction environment and promote the efficient progress of the reaction. At the same time, in the separation and purification stage of the product, the difference in solubility can also be used to achieve the separation of the target product and impurities by means of extraction.

The density is [X] g/cm ³, which reflects the mass per unit volume of the substance. In the measurement process of chemical production, density is crucial. Through the determination of density and volume, the quality of substances can be accurately obtained, and the ratio of reactants can be guaranteed to be accurate, thereby ensuring the stability and consistency of product quality.

In addition, 2-chloro-4-fluorobenzyl cyanide is volatile and will slowly evaporate into the air at room temperature. This requires that during storage and use, it is necessary to pay attention to ventilation and ventilation to prevent it from accumulating in a limited space and causing safety hazards, such as flammable and explosive risks or harm to human health.

In summary, the many physical properties of 2-chloro-4-fluorobenzyl cyanide play an indispensable role in its production, storage, transportation and application. In-depth understanding and rational utilization of these properties is of great significance to the development of related fields.

2-Chloro-4-fluorobenzyl the chemistry of cyanide

2-Chloro-4-fluorobenzyl cyanide, this is an organic compound. Its chemical properties are unique and related to organic synthesis and reactivity.

In terms of its stability, the cyanyl group (-CN) has high stability in the molecular structure, because the carbon atom and the nitrogen atom are connected by three bonds, and the bond energy is quite large. Although the chlorine atom (-Cl) and the fluorine atom (-F) are electron-withdrawing groups, which have an impact on the distribution of molecular electron clouds, the stability of the cyanyl group is still dominant. Therefore, 2-chloro-4-fluorobenzyl cyanide can remain relatively stable at room temperature and pressure without special chemical reagents or conditions.

When it comes to reactivity, the first is nucleophilic substitution. Both chlorine and fluorine atoms can be used as leaving groups. Due to the electron-absorbing induction effect of halogen atoms, benzyl carbon atoms are partially positively charged and vulnerable to nucleophilic reagents. Among them, chlorine atoms are easier to leave than fluorine atoms, because the carbon-chlorine bond length is longer and the bond energy is relatively low. Nucleophilic reagents such as sodium alcohol and amines can react with 2-chloro-4-fluorobenzyl cyanide to form new organic compounds, which are widely used in the field of organic synthesis.

Furthermore, cyanyl groups can participate in a variety of reactions. For example, in hydrolysis reactions, under acidic or alkaline conditions, cyanyl groups can be gradually hydrolyzed to carboxyl groups (-COOH). Hydrolysis under acidic conditions results in amide intermediates, and further hydrolysis to carboxylic acids; under alkaline conditions, the hydrolysis process is also similar, but the reaction mechanism is slightly different. This hydrolysis reaction is an important way to prepare carboxyl-containing organic compounds.

Cyanyl groups can also participate in reduction reactions. With appropriate reducing agents, such as lithium aluminum hydride (LiAlH), cyanyl groups can be reduced to amine groups (-NH2O). This reaction also plays an important role in the preparation of amine-containing compounds.

2-Chloro-4-fluorobenzyl cyanide plays a key role in the field of organic synthetic chemistry due to the characteristics of halogen atoms and cyano groups in its structure. Its stability and diverse reactivity provide rich possibilities for the synthesis of complex organic molecules, and can be widely used in the preparation of organic compounds in many fields such as medicine, pesticides, materials, etc.

What is the production method of 2-Chloro-4-fluorobenzyl cyanide?

The method of making 2-chloro-4-fluorobenzyl cyanide has been around since ancient times. In the spirit of "Tiangong Kaiwu", we should follow the scientific method, analyze its steps and describe its skills.

First, use 2-chloro-4-fluorotoluene as the starting material, which is the foundation. In the reactor, add an appropriate amount of initiator, usually such as azobisisobutyronitrile. Then heat up to a suitable degree, about 100-120 degrees Celsius. At this time, slowly introduce chlorine gas to make 2-chloro-4-fluorotoluene undergo side chain chlorination reaction, and 2-chloro-4-fluorobenzyl chloride can be obtained. This step requires precise temperature control and uniform ventilation to avoid side reactions.

times, take the prepared 2-chloro-4-fluorobenzyl chloride and react with sodium cyanide in an appropriate solvent. Commonly used solvents, such as N, N-dimethylformamide (DMF), have good solubility to the reaction system and can promote ion exchange. The reaction temperature should be maintained at 80-100 degrees Celsius, and the two should be stirred continuously to make full contact and nucleophilic substitution reaction occurs. After this step, the chlorine atom of 2-chloro-4-fluorobenzyl chloride is replaced by a cyanyl group, and then 2-chloro-4-fluorobenzyl cyanide is obtained.

After the reaction is completed, the product needs to be separated and purified. First, the solvent and unreacted raw materials are removed by vacuum distillation. Then, by column chromatography, using silica gel as the stationary phase, a suitable eluent, such as a mixture of petroleum ether and ethyl acetate, is prepared in different proportions to separate the product from impurities, and pure 2-chloro-4-fluorobenzyl cyanide can be obtained.

This is a common preparation method of 2-chloro-4-fluorobenzyl cyanide. Following this step, the conditions can be controlled to obtain a product with good yield.

What are the precautions for 2-Chloro-4-fluorobenzyl cyanide in storage and transportation?

2-Chloro-4-fluorobenzyl cyanide is a chemical substance. During storage and transportation, the following things must be paid attention to.

First safety protection. Because of its toxicity and irritation, contact can cause human damage. When storing, operators must wear professional protective clothing, protective gloves, goggles and gas masks to prevent skin contact and inhalation. During transportation, transporters should also strictly abide by safety procedures to ensure their own protection.

Second words storage conditions. It should be placed in a cool and ventilated warehouse, away from fire and heat sources. This substance is heated or causes chemical reactions, resulting in dangerous conditions. And should be stored separately from oxidizing agents, acids, alkalis, etc., do not mix storage to prevent interaction and accidents. The warehouse should also be equipped with suitable materials to contain leaks in case of emergency.

The other is the transportation requirement. Before transportation, be sure to ensure that the packaging is complete and well sealed. Select appropriate means of transportation and follow relevant transportation regulations. During transportation, it should be protected from sun exposure, rain and high temperature. If it is road transportation, follow the specified route and do not stop in residential areas and densely populated areas. When rail transportation, it is also necessary to go through transportation formalities in accordance with regulations.

In addition, whether it is storage or transportation, the substance should be clearly marked, indicating its name, danger and other important information, so that relevant personnel can identify and take correct countermeasures. At the same time, relevant places should be equipped with corresponding emergency treatment equipment and equipment, such as fire extinguishers, eye washers, first aid medicines, etc., so that in the event of an accident, rescue actions can be taken quickly to reduce the degree of harm.