2 Cyano 3 2 3 Chlorophenyl Ethyl Pyridine
pyridine pyrrole pyrazine piperidine piperazine

2-Cyano,3-[2-(3'Chlorophenyl)] Ethyl Pyridine

    Specifications

    HS Code

    922474

    Chemical Formula C14H11ClN2
    Molecular Weight 242.708 g/mol
    Appearance Solid (usually)
    Physical State At Room Temperature Solid
    Melting Point Data may vary, check specific sources
    Boiling Point Data may vary, check specific sources
    Solubility In Water Low solubility
    Solubility In Organic Solvents Soluble in some organic solvents like dichloromethane
    Density Data may vary, check specific sources
    Odor Typically odorless or with a faint, characteristic smell

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    General Information
    Where to Buy 2-Cyano,3-[2-(3'Chlorophenyl)] Ethyl Pyridine in China?
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    Frequently Asked Questions

    As a leading 2-Cyano,3-[2-(3'Chlorophenyl)] Ethyl Pyridine 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 chemical properties of 2-Cyano, 3- [2- (3'Chlorophenyl) ] Ethyl Pyridine
    2-Cyano, 3- [2- (3 '-chlorophenyl) ] ethylpyridine, this is an organic compound. Its chemical properties are quite complex, let me explain in detail.
    Looking at its structure, cyano (-CN) confers unique reactivity to this compound. Cyanyl is nucleophilic and can participate in many nucleophilic substitution reactions. Under suitable conditions, cyanyl can be hydrolyzed and converted to carboxyl (-COOH). This reaction is often a key step in organic synthesis. It can introduce acidic functional groups into compounds, thereby changing their chemical and physical properties.
    Furthermore, the pyridine ring is also an important structural part. The pyridine ring is aromatic, and the electron cloud distribution is special, which makes the nitrogen atom on the pyridine ring appear weakly basic. This basic property allows the compound to react with acids to form corresponding salts. The pyridine ring can also act as an electron receptor to participate in charge transfer-related reactions, which may have potential applications in the field of organic optoelectronic materials.
    And the substituent 3- [2- (3 '-chlorophenyl) ] ethyl has a significant impact on the properties of the compound. Chlorine atoms on the benzene ring have a large electronegativity and an electron-absorbing induction effect, which can reduce the electron cloud density of the benzene ring, which in turn affects the electrophilic substitution reaction activity on the benzene ring. The steric hindrance of this substituent also plays a role in the reaction selectivity of the compound. When a chemical reaction occurs, the reactivity in the larger area of the steric hindrance may decrease, which prompts the reaction to proceed more in the small area of the steric hindrance.
    In summary, the chemical properties of 2-cyano, 3- [2- (3 '-chlorophenyl) ] ethylpyridine are determined by the synergistic structure of its various parts, and may show various chemical reactions and potential applications in the fields of organic synthesis, materials science, etc.
    What are the main uses of 2-Cyano, 3- [2- (3'Chlorophenyl) ] Ethyl Pyridine
    2-Cyano, 3- [2- (3 '-chlorophenyl) ] ethylpyridine, this is an organic compound. It has a wide range of uses in the field of medicine, or is a key intermediate for the synthesis of drugs with specific biological activities. Due to the structural characteristics of chlorophenyl and pyridine, it can endow drugs with unique pharmacological properties, and can participate in a variety of drug chemical synthesis pathways, helping to develop therapeutic drugs for specific diseases.
    In the field of materials science, it also has important uses. Or it can be used as a building unit of functional materials. With its special chemical structure, it can be introduced into polymer materials to give materials unique properties such as optical, electrical or thermal properties. For example, it can improve the fluorescence properties of materials and be applied to photoelectric display materials; or it can enhance the stability of materials and be used in high-performance engineering plastics.
    In the field of agricultural chemistry, it may also play a role. It may be used to synthesize new pesticides that exhibit biological activity against specific pests or pathogens by virtue of their chemical structure, thereby realizing the development of high-efficiency and low-toxicity pesticides, contributing to the sustainable development of agriculture, providing effective protection for crops, and reducing the negative impact on the environment.
    With its unique chemical structure, this compound has potential application value in the fields of medicine, materials science and agricultural chemistry, providing new opportunities for research and development in many fields.
    What is the synthesis method of 2-Cyano, 3- [2- (3'Chlorophenyl) ] Ethyl Pyridine
    The synthesis of 2-cyano-3- [2 - (3 '-chlorophenyl) ] ethylpyridine is a key technique in the field of chemical synthesis. To obtain this compound, the following steps can be followed.
    First, choose the appropriate starting material. For example, a compound containing 3-chlorophenyl as the starting base is combined with a pyridine derivative with a suitable active group. Usually, 3-chlorophenyl compounds with reactive substituents, such as 3-chlorophenyl halide, can be selected. This halogen atom is highly active and is easy to participate in subsequent reactions. Pyridine derivatives also need to have groups that can react with 3-chlorobenzene derivatives, such as halogen atoms, hydroxyl groups or amino groups.
    For the second time, choose suitable reaction conditions. It is often better to react in an inert gas atmosphere to prevent the raw materials and products from being oxidized. The choice of reaction solvent is also extremely important. Organic solvents such as N, N-dimethylformamide (DMF), dichloromethane, etc. are commonly used, which can effectively dissolve the raw materials and catalysts without interfering with the reaction.
    Furthermore, a catalyst is added to accelerate the reaction process. Depending on the reaction path, metal catalysts can be selected, such as palladium catalysts, which are effective in catalyzing the coupling reaction of halogenated aromatics and nitrogen-containing heterocycles; or alkali catalysts, such as potassium carbonate, sodium carbonate, etc., can promote the occurrence of nucleophilic substitution reactions.
    Then, the reaction is carried out at a specific temperature. The regulation of temperature is related to the reaction rate and product selectivity. Generally speaking, the reaction temperature may be between room temperature and 150 ° C, depending on the specific reaction mechanism and raw material activity. During the reaction process, it needs to be monitored by means of thin chromatography (TLC) or high-performance liquid chromatography (HPLC). When the raw material is exhausted or the expected reaction level is reached, the reaction is terminated. At the end of
    , the reaction is completed, and the product is separated and purified. First, the extraction operation can be carried out with organic solvent and aqueous phase to enrich the product in the organic phase. Then, the column chromatography method is used to select suitable silica gel column and eluent to separate the product from impurities, and finally obtain high purity 2-cyano-3- [2 - (3 '-chlorophenyl) ] ethylpyridine.
    2-Cyano, 3- [2- (3'Chlorophenyl) ] Ethyl Pyridine What to pay attention to when storing
    2-Cyano, 3- [2- (3 '-chlorophenyl) ] ethylpyridine, this is a special chemical substance. When storing, many points need to be paid attention to carefully.
    Bear the brunt, temperature control is essential. It should be kept in a cool place to avoid the disturbance of high temperature. High temperature can easily cause its chemical properties to be unstable, or cause decomposition and deterioration. Due to high temperature, molecular movement can be exacerbated, which makes chemical reactions more likely to occur, endangering the original characteristics of the substance.
    Secondly, the influence of humidity should not be underestimated. Store in a dry place, beware of moisture. Moisture easily interacts with the substance, or causes adverse reactions such as hydrolysis. Water molecules may intervene in its molecular structure and change its chemical composition and properties.
    Furthermore, the light factor should not be ignored. It should be stored in a dark place, such as in a dark container, or in a dark place. Light, especially strong light, may cause luminescent chemical reactions to cause it to deteriorate. Light energy can provide the energy required for the reaction, causing molecular bonds to break and recombine.
    In addition, the substance may have certain toxicity or irritation. During storage, make sure that the container is well sealed to prevent leakage. Once leaked, it not only poses a threat to the environment, but also may endanger personal safety. If accidentally touched, it may cause physical discomfort.
    At the same time, the storage place should be kept away from fire sources, heat sources and all kinds of flammable and explosive materials. Due to its chemical properties, there may be a latent risk of flammable and explosive. If the fire source or heat source is close, a little carelessness may cause a dangerous situation.
    And the storage area should be well ventilated. In the event of leakage, ventilation can disperse harmful gases in time and reduce the risk factor. Good ventilation also helps to maintain the stability of the storage environment.
    When storing, it should also be well marked. Clearly mark the name, characteristics, storage conditions and other key information of the substance. In this way, it is easy to access and manage, and avoid improper use due to mistaken recognition.
    What is the market price of 2-Cyano, 3- [2- (3'Chlorophenyl) ] Ethyl Pyridine
    I look at your question, and I am inquiring about the market price of 2-cyano, 3- [2 - (3 '-chlorophenyl) ] ethylpyridine. However, the price of this chemical cannot be answered immediately. The price of the chemical is affected by many factors, such as the price of raw materials, the difficulty of preparation, the supply and demand of the market, and the purity of the product.
    First talk about the price of raw materials. The preparation of this chemical requires specific raw materials. If the raw materials are scarce, or the price increases due to natural disasters or government regulations, the production cost of this chemical will increase, and its market price will also be higher.
    Times and the difficulty of preparation. If the preparation method is cumbersome, high-precision equipment and specialized technology are required, and the process consumes a lot of manpower and material resources, and the yield is not high, the cost will rise and the price will also rise.
    Also discuss the supply and demand of the market. If the market demand for this product is strong, but the supply is limited, according to the reason of supply and demand, the price will rise; on the contrary, if the demand is low and the supply is excessive, the price may fall.
    Furthermore, the purity of the product has a great impact. For high purity, the preparation is more difficult, the cost is higher, and the price is much higher than that of low purity.
    According to the theory of "Tiangong Kaiwu", the price of various products is determined by the difficulty of creation and the urgency of supply and demand. This chemical is no exception. Therefore, in order to determine the market price, it is necessary to carefully investigate the raw material market, preparation process, market supply and demand, and purity standards, or consult chemical industry companies and professional market research institutions to obtain a more accurate price.