2 Chloro 1 4 Fluorobenzyl 1h Benzimidazole
quinoline thiophene imidazole thiazole

2-Chloro-1-(4-Fluorobenzyl)-1H-Benzimidazole

    Specifications

    HS Code

    596298

    Chemical Formula C14H10ClFN2
    Molecular Weight 260.698 g/mol
    Appearance Typically a solid (physical state depends on conditions)
    Melting Point Data may vary, needs experimental determination
    Boiling Point Data may vary, needs experimental determination
    Solubility Solubility characteristics vary with solvents
    Density Data may vary, needs experimental determination
    Pka Data may vary, needs experimental determination
    Logp Data may vary, needs experimental determination
    Vapor Pressure Data may vary, needs experimental determination

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    General Information
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    Frequently Asked Questions

    As a leading 2-Chloro-1-(4-Fluorobenzyl)-1H-Benzimidazole 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-Chloro-1- (4-Fluorobenzyl) -1H-Benzimidazole?
    2-Chloro-1- (4-fluorobenzyl) -1H-benzimidazole is an organic compound with unique chemical properties. Its molecule contains benzimidazole core structure, which endows the compound with various reactivity. Because the benzimidazole ring is aromatic, it has high chemical stability, and the nitrogen atom can participate in a variety of chemical reactions, such as nucleophilic substitution, coordination reaction, etc. < Br >
    2 -chlorine atom in the molecule is an active check point, because of the large electronegativity of chlorine atom, the C-Cl bond has polarity, vulnerable to attack by nucleophilic reagents, nucleophilic substitution reaction occurs, such as being substituted by hydroxyl groups, amino groups, etc., to form a series of derivatives, which are widely used in the field of organic synthesis.
    1 - (4 -fluorobenzyl) part, benzyl is a benzene ring and methylene linked structure, which has a certain power supply effect, which can affect the electron cloud density of benzimidazole ring and change its reactivity. The 4-fluorine atom replaces the benzyl benzene ring, the fluorine atom is highly electronegative, and has a strong electron-absorbing induction effect, which not only affects the distribution of benzyl electron clouds, but also affects the physical and chemical properties of the whole molecule, such as molecular polarity, solubility, and in some reactions affect the selectivity of the reaction check point.
    This compound may also exhibit acidity and alkalinity, because the benzimidazole ring nitrogen atom can accept the proton to be basic, and at the same time, its acidity and alkalinity will change under the influence of the substituent. Under different acid and base conditions, the molecules exist in different forms or have differences, which in turn affect their reactivity and solubility.
    In addition, the spectral properties of this compound are also worthy of attention. For example, in infrared spectroscopy, the vibration absorption peaks of different chemical bonds can be used for structural identification; nuclear magnetic resonance spectroscopy can provide information on the atomic chemical environment of hydrogen, carbon and other atoms in molecules, and help accurate structure analysis.
    In short, 2-chloro-1- (4-fluorobenzyl) -1H-benzimidazole has rich chemical properties and has potential application value in organic synthesis, pharmaceutical chemistry and other fields.
    What are the common uses of 2-Chloro-1- (4-Fluorobenzyl) -1H-Benzimidazole?
    2-Chloro-1- (4-fluorobenzyl) -1H-benzimidazole, a common use of this substance, is often involved in the field of medicine and pesticides.
    In the process of medicine, it is often the key intermediate for the creation of new drugs. The structure of Geinbenzimidazole has unique physiological activities and can interact with many targets in organisms. For example, some anti-parasitic drugs, by means of structural modification of such compounds, optimize their affinity and selectivity to specific enzymes or receptors of parasites, and achieve the purpose of efficient deworming. Or in the development of anti-cancer drugs, this structure is modified so that it can accurately act on targets related to cancer cell proliferation and apoptosis, and inhibit cancer cell growth.
    As for the pesticide category, it is also an important raw material. After rational design and modification, pesticides with high insecticidal and bactericidal properties can be prepared. For example, for the specific physiological mechanism of some crop pests, the compound is used as a basis to develop insecticides, interfere with the pest nervous system or physiological metabolic process, and achieve pest control. In terms of fungicides, it can act on the cell wall, cell membrane or key metabolic enzymes of pathogenic bacteria, inhibit the growth and reproduction of pathogenic bacteria, and protect the healthy growth of crops.
    Due to its structural characteristics, this compound has broad application prospects in the field of medicine and pesticide creation, and has made great contributions to protecting human health and agricultural harvest.
    What are the synthesis methods of 2-Chloro-1- (4-Fluorobenzyl) -1H-Benzimidazole?
    The synthesis of 2-chloro-1- (4-fluorobenzyl) -1H-benzimidazole is an important research in the field of organic synthesis. Today, in ancient French proverbs, the path of its synthesis is described.
    First, benzimidazole is often used as the starting material. First, benzimidazole is substituted with halobenzyl compounds under appropriate reaction conditions. Among the halobenzyl, 4-fluorobenzyl halogen is the key reagent. In this reaction, the solvent, such as N, N-dimethylformamide (DMF), should be carefully selected, because its polarity is moderate, it can effectively promote the reaction. It is necessary to add an appropriate amount of alkali, such as potassium carbonate, to assist the halogen atom of halobenzyl to leave, so that the nitrogen atom of benzimidazole undergoes nucleophilic substitution with it, thereby introducing 4-fluorobenzyl.
    Second, synthesize 2-chloro-1- (4-fluorobenzyl) -1H-benzimidazole, and also use o-phenylenediamine and 4-fluorophenylacetic acid as starting materials. O-phenylenediamine and 4-fluorophenylacetic acid first undergo a condensation reaction to form an intermediate product. This condensation reaction may be carried out in the presence of suitable catalysts, such as some acidic catalysts, to promote the reaction of the two. Then, the intermediate product is chlorinated to introduce chlorine atoms at specific positions. In the chlorination process, the chlorination reagents used are very critical, such as phosphorus oxychloride, etc., and the reaction temperature and time need to be strictly controlled to ensure that the chlorination reaction occurs accurately at the target location and avoid side reactions such as excessive chlorination.
    Third, other compounds with similar structures are also used as starting materials and converted through multi-step reactions. However, regardless of the route, it is necessary to carefully control the reaction conditions, such as temperature, pH, reaction time, etc., to obtain a higher yield and purity of 2-chloro-1- (4-fluorobenzyl) -1H-benzimidazole. After each step of the reaction, it is often necessary to perform separation and purification operations, such as column chromatography, recrystallization, etc., to remove impurities and improve product quality.
    What is the price range of 2-Chloro-1- (4-Fluorobenzyl) -1H-Benzimidazole in the market?
    The price of 2-chloro-1- (4-fluorobenzyl) -1H-benzimidazole in the market is difficult to determine. This is due to the intertwining of various factors, resulting in fluctuations in its price range.
    First, the source and cost of the material have a lot to do with it. If the raw materials required for its preparation are easy to obtain, the supply is plentiful, and the price may be stable and flat; if the raw materials are rare and difficult to obtain, the price will rise. If there is a disaster in the raw material production area, the output will drop sharply, which will lead to a soaring cost, which will then increase the price of 2-chloro-1- (4-fluorobenzyl) -1H-benzimidazole.
    Second, the clumsiness of the manufacturing process is also the main reason. The exquisite manufacturing process can increase the yield and reduce the consumption, so that the cost can be reduced and the price can be reduced; if the manufacturing process is crude, the production efficiency is low and the consumption is large, and the price will be high. The creation of new technologies, if the process can be simplified, the quality and quantity can be improved, the price can often be changed.
    Third, the supply and demand of the city determines the price. When demand exceeds supply, the price will rise; if supply exceeds demand, the price will fall. If pharmaceutical research and development takes off, the demand for this product will increase sharply, and the production will be difficult to respond quickly, the price will rise; on the contrary, if the number of users decreases and the production is too high, the price will fall.
    Fourth, the regulation of government also has an impact. Changes in taxes and environmental protection regulations can affect their costs and prices. Taxes increase, costs increase and prices rise; environmental protection becomes stricter, and enterprises are urged to invest in environmental protection, which also increases costs or causes prices to rise.
    To sum up, the market price of 2-chloro-1- (4-fluorobenzyl) -1H-benzimidazole is variable, subject to various constraints such as source materials, manufacturing, supply and demand, and political regulations. Its price often varies from time to time and fluctuates indeterminately. It is difficult to determine the range of its price.
    What are the precautions for 2-Chloro-1- (4-Fluorobenzyl) -1H-Benzimidazole during storage and transportation?
    2-Chloro-1- (4-fluorobenzyl) -1H-benzimidazole is an organic compound. When storing and transporting, many matters need to be paid attention to.
    In terms of storage, the first environment is dry. This compound is susceptible to moisture. If the environment is humid, it may cause reactions such as hydrolysis, damage the structure and reduce the purity and quality. Therefore, it should be placed in a dry, well-ventilated place, away from water sources and water vapor.
    Temperature is also critical. It should be stored in a suitable low temperature environment, usually 2-8 ° C. High temperature or reduce the stability of the compound, accelerate decomposition or initiate other chemical reactions. And it is necessary to avoid direct sunlight. Light may also cause luminescent chemical reactions and change its chemical properties.
    Furthermore, the storage place should be kept away from oxidants and reducing agents. Because of its specific chemical activity, contact with oxidation and reducing agents, or trigger violent chemical reactions, poses a safety hazard.
    When transporting, the packaging must be solid and reliable. Pack in a special sealed container to prevent leakage. The material of the container must be compatible with the compound and do not react with it.
    The transportation process should be maintained smoothly to avoid vibration and collision. Violent vibration or damage to the package will cause compound leakage. And the transportation environmental conditions should also be strictly controlled, and the temperature and humidity are similar to the storage requirements.
    Transportation personnel need to be professionally trained and familiar with the characteristics of the compound and emergency treatment methods. In the event of leakage and other accidents, they can respond quickly and properly to reduce harm. In this way, 2-chloro-1- (4-fluorobenzyl) -1H-benzimidazole is guaranteed to be safe and stable during storage and transportation.