2 Chloro 5 Fluorobenzylcyanide
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
2-Chloro-5-fluorobenzylcyanide
Chemical Formula C8H5ClFN
Molar Mass 169.58 g/mol
Physical State At Room Temp Likely a solid or liquid
Solubility In Water Low, due to non - polar nature of the benzene ring and hydrophobic groups
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, acetone, chloroform
Vapor Pressure Low (estimation based on its likely low volatility from structure)
Chemical Formula C8H5ClFN
Molar Mass 169.583 g/mol
Appearance Solid (presumably, based on similar compounds)
Solubility In Water Low solubility in water, as it is an organic compound with non - polar groups
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, acetone, etc.
Vapor Pressure Low vapor pressure due to its relatively high molar mass and solid nature
FAQ

What is the chemistry of 2-Chloro-5-fluorobenzylcyanide?

2-Chloro-5-fluorobenzyl cyanide, this is an organic compound. In terms of physical properties, it is mostly liquid or solid under normal conditions, and the color state often varies with purity, or is colorless and transparent, or has a slight color. Its odor is unique, but the specific description needs to be personally observed to be clear.

As for chemical properties, its molecules contain chlorine atoms, fluorine atoms and cyano groups, and each group gives this compound a specific activity. Chlorine atoms and fluorine atoms have electron-absorbing properties, which can reduce the electron cloud density of benzene rings and affect the electrophilic substitution reaction activity on benzene rings. Compared with benzene rings replaced by halogen-free atoms, the reaction activity may change. The cyanyl group is active and can participate in a variety of reactions. For example, under appropriate conditions, the cyanyl group can be hydrolyzed into a carboxyl group and converted into 2-chloro-5-fluorobenzoic acid; it can also be converted into the corresponding amine group by reduction reaction to generate 2-chloro-5-fluorobenzyl amine.

In addition, this compound has good solubility in some organic solvents due to its halogen atom and cyanyl group. It is often used as an intermediate in the field of organic synthesis. With the help of its group activity, more complex organic molecular structures can be constructed to meet the needs of pharmaceutical chemistry, materials science and other fields.

What are the main uses of 2-Chloro-5-fluorobenzylcyanide?

2-Chloro-5-fluorobenzyl cyanide, an important intermediate in organic synthesis, is widely used in medicine, pesticides and other fields.

In the field of medicine, one of its key uses is to participate in the synthesis of various drugs. The construction of many drug molecules requires the unique chemical structure of this compound. For example, in the development of some anti-cancer drugs, 2-chloro-5-fluorobenzyl cyanide can be used as a starting material to precisely construct a molecular skeleton with specific pharmacological activities through a series of chemical reactions. Because it contains chlorine, fluorine and other atoms, it can change the physical and chemical properties of drug molecules, such as lipophilicity and stability, which in turn affect the absorption, distribution, metabolism and excretion process of drugs, and improve drug efficacy.

In the field of pesticides, it also plays an important role. It can be used to synthesize new pesticides, fungicides and other pesticide products. Due to its structural characteristics, it can endow pesticides with specific biological activities and exhibit high-efficiency inhibition or killing effects on pests or pathogens. For example, interference with the nerve conduction system of specific pests or the cell wall synthesis process of pathogens can achieve the purpose of controlling pests and diseases. Compared with traditional pesticides, such pesticides based on 2-chloro-5-fluorobenzyl cyanide synthesis may be more selective and environmentally friendly, reducing the impact on non-target organisms and reducing environmental pollution.

Furthermore, in organic chemistry research, 2-chloro-5-fluorobenzyl cyanide is used as a reaction substrate, providing an opportunity to explore new chemical reactions and synthesis methods. Chemists can use its active groups to carry out various nucleophilic substitution, addition and other reactions, expand the boundaries of organic synthesis chemistry, develop more efficient and green synthesis strategies, and lay the foundation for the synthesis of more complex organic compounds.

What are 2-Chloro-5-fluorobenzylcyanide synthesis methods?

The synthesis of 2-chloro-5-fluorobenzyl cyanide is very important. In the past, many parties have investigated this synthesis method, as follows.

First, it can be obtained by reacting 2-chloro-5-fluorobenzyl halide with a cyanide reagent. In a suitable reaction vessel, put 2-chloro-5-fluorobenzyl halide, which has high halogen atom activity and can react with cyanide reagents. Commonly used cyanide reagents, such as potassium cyanide, sodium cyanide, etc. When reacting, pay attention to the choice of reaction temperature and solvent. If the temperature is too high, or cause more side reactions; if the temperature is too low, the reaction rate will be slow. Solvents are also particular, and polar aprotic solvents such as dimethylformamide (DMF) and dimethyl sulfoxide (DMSO) are commonly used. Such solvents can improve the solubility and reactivity of cyanide reagents and promote the smooth progress of the reaction.

Second, 2-chloro-5-fluorobenzoic acid is used as the starting material. First, 2-chloro-5-fluorobenzoic acid is converted into its acid chloride form, which can be achieved by reacting with reagents such as thionyl chloride. After the acid chloride is obtained, it reacts with ammonia to form an amide, and then dehydrates to form a nitrile, which is to obtain 2-chloro-5-fluorobenzyl cyanide. In this process, the control of the reaction conditions at each step is very critical. For the preparation of acid chloride, the reaction requires an anhydrous environment, otherwise the acid chloride is easy to hydrolyze. For the dehydration step of the amide, a suitable dehydrating agent and reaction temperature are also required to obtain the ideal yield.

Third, through the nucleophilic substitution reaction path on the aromatic ring. Select a suitable nucleophilic reagent with a cyano group and react with the specific activated 2-chloro-5-fluorobenzene derivative. There are various methods for activating aromatic rings, and the electron cloud density of aromatic rings can be changed by introducing suitable substituents to enhance their nucleophilic substitution activity. This path requires in-depth understanding of the mechanism of aromatic ring activation and nucleophilic substitution, and precise control of the reaction conditions to obtain the target product.

All these synthesis methods have their own advantages and disadvantages. In practical applications, the best one should be selected according to the availability of raw materials, the difficulty of reaction, cost considerations and many other factors.

2-Chloro-5-fluorobenzylcyanide What are the precautions during storage and transportation?

2-Chloro-5-fluorobenzyl cyanide is an organic chemical substance. During storage and transportation, many things must be paid attention to to to avoid accidents.

The first thing to pay attention to is storage conditions. This substance should be stored in a cool, dry and well-ventilated place, away from fire and heat sources. Because of its certain chemical activity, high temperature is prone to chemical reactions, or there is a risk of combustion or explosion. The warehouse temperature should be controlled within a specific range to prevent temperature fluctuations from changing the properties of the substance. And keep away from oxidants, acids, bases, etc., because of their contact or violent reaction. Be sure to store it separately, do not mix it, and the storage area should be prepared with suitable materials to contain leaks. < Br >
The second is the attention of transportation. Before transportation, ensure that the packaging is complete and the loading is safe. Packaging materials need to have good sealing and corrosion resistance to prevent material leakage during transportation. When transporting, use compliant means of transportation, and label and declare in accordance with relevant regulations. During transportation, it must be protected from exposure to the sun, rain and high temperature. Summer transportation should be selected in the morning and evening to avoid high temperature. Drivers and escorts must also be familiar with the characteristics of the substance and emergency treatment methods. During the journey, check the condition of the goods frequently. If there is any abnormality such as leakage, take measures quickly.

Furthermore, whether it is storage or transportation, a complete safety management system and emergency plan are required. Management personnel should be professionally trained and familiar with material characteristics and safety operation procedures. Periodically inspect and maintain storage facilities and transportation tools to ensure their good safety performance. In the event of a leak or other accident, emergency plans can be quickly activated to reduce hazards.

2-Chloro-5-fluorobenzylcyanide impact on the environment and human health

2-Chloro-5-fluorobenzyl cyanide, this is a chemical substance. Its impact on the environment and human health cannot be ignored.

In terms of the environment, if this substance enters the natural water body, it may be polluted. Aquatic organisms are extremely sensitive to it, or its physiological functions are damaged due to it. If the gill tissue of fish is irritated or irritated, it will cause poor respiration, and the population may decrease. And it is difficult to degrade in the soil, accumulates for a long time, or changes the physical and chemical properties of the soil, inhibits plant growth, and causes ecological imbalance.

It is related to human health and is very harmful to the body through inhalation, skin contact or accidental ingestion. When inhaled, it irritates the respiratory tract, causing cough, asthma, prolonged exposure to this environment, or increases the risk of respiratory diseases. Skin contact can cause allergies, redness, swelling, itching, and in severe cases, ulceration. Accidental ingestion can damage the digestive system. Nausea, vomiting, and abdominal pain are common symptoms, even life-threatening.

It may interfere with normal metabolism at the cellular level, affect gene expression, and pose a potential carcinogenic and teratogenic risk. Therefore, the production, use, and disposal of 2-chloro-5-fluorobenzyl cyanide must be handled with caution to reduce its harm to the environment and human health.