2 Chloromethyl 1 Methyl 1h Benzo D Imidazole
quinoline thiophene imidazole thiazole

2-(chloromethyl)-1-methyl-1H-benzo[d]imidazole

    Specifications

    HS Code

    219265

    Chemical Formula C9H9ClN2
    Molar Mass 180.64 g/mol
    Appearance Solid (presumably, based on common benzoimidazole derivatives)
    Physical State At Room Temperature Solid
    Solubility In Water Limited solubility expected (due to non - polar aromatic structure)
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform (common for similar aromatic compounds)

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    Frequently Asked Questions

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    What are the physical properties of 2- (chloromethyl) -1-methyl-1H-benzo [d] imidazole
    2 - (chloromethyl) -1 - methyl - 1H - benzo [d] imidazole is an organic compound with unique physical properties.
    Looking at its appearance, at room temperature and pressure, it is mostly white to light yellow crystalline powder, which makes it easy to handle and operate in many scenarios.
    When it comes to the melting point, it is about 150-155 ° C. As a material characteristic, the melting point is crucial for the identification and purification of this compound. At this temperature, the substance melts from a solid state to a liquid state, reflecting the strength of intermolecular forces.
    Its solubility is also characterized. Slightly soluble in water, but soluble in common organic solvents, such as ethanol, dichloromethane, N, N-dimethylformamide, etc. In ethanol, with the increase of temperature, the solubility increases. This solubility is related to the molecular structure. The presence of benzimidazole ring and methyl and chloromethyl in the molecule makes it hydrophobic to a certain extent, so it is insoluble in water, but easily soluble in organic solvents.
    The compound has good stability and can maintain its chemical structure under normal storage and use conditions. However, it will also react chemically when exposed to strong oxidizing agents, strong acids or strong bases. In a strong acid environment, the nitrogen atom of the benzimidazole ring is protonated; when exposed to strong oxidizing agents, it may cause oxidation of the substituent on the ring.
    In addition, 2 - (chloromethyl) - 1 - methyl - 1H - benzo [d] imidazole is volatile, and a small amount evaporates into the air in heating or high concentration environments. Pay attention to ventilation during operation to ensure safety.
    What are the chemical properties of 2- (chloromethyl) -1-methyl-1H-benzo [d] imidazole
    2-%28chloromethyl%29-1-methyl-1H-benzo%5Bd%5Dimidazole, this is the name of the chemical substance, translated in modern chemical nomenclature, that is, 2 - (chloromethyl) - 1 - methyl - 1H - benzo [d] imidazole. Its chemical properties are very important and are related to many chemical applications.
    Looking at its structure, this compound contains a benzimidazole parent nucleus with chloromethyl on one side and methyl on the other side. The benzimidazole parent nucleus gives it a certain aromaticity and stability. The aromaticity gives the molecule a special electron cloud distribution, which makes its chemical properties different from ordinary aliphatic compounds. The two substituents, chloromethyl and methyl, also have a great influence on its properties.
    The chlorine atom of chloromethyl has strong electronegativity, which makes chloromethyl an electron absorber. This property affects the distribution of the molecular electron cloud, which changes the electron cloud density on the benzimidazole ring, which in turn affects its electrophilic substitution activity. Usually, the electron-absorbing group will reduce the electron cloud density of the benzene ring, making the electrophilic substitution reaction more difficult. However, under certain conditions, the chlorine atom of chloromethyl can undergo nucleophilic substitution reaction, because it can be used as a leaving group and can be attacked and replaced by nucleophilic reagents. This is one of the important reaction characteristics of this compound.
    Methyl is the power supply subgroup, which increases the electron cloud density of the benzimidazole ring relative to the electron- Although the electron effect is relatively weak, it also affects the molecular reactivity, and interacts with chloromethyl to balance and jointly determine the chemical properties of the compound. Overall, the interaction of various parts in the structure of 2 - (chloromethyl) - 1 - methyl - 1H - benzo [d] imidazoline may have unique uses in organic synthesis, medicinal chemistry and other fields. It can be used as a key intermediate to participate in various chemical reactions and construct more complex organic molecular structures.
    What are the common synthesis methods of 2- (chloromethyl) -1-methyl-1H-benzo [d] imidazole
    2-%28chloromethyl%29-1-methyl-1H-benzo%5Bd%5Dimidazole, that is, 2 - (chloromethyl) - 1 - methyl - 1H - benzo [d] imidazole, the common synthesis method is as follows:
    First, the starting material is o-phenylenediamine and formic acid. Put the o-phenylenediamine and formic acid into the reactor in a certain proportion, heat it to an appropriate temperature, usually between 100-150 ° C, and carry out the condensation reaction. This step aims to make the two amino groups of o-phenylenediamine condensate with formic acid to form a benzimidazole ring structure to generate 1 - methylbenzimidazole. During the reaction, constant stirring is required to promote the full mixing of materials and speed up the reaction process.
    The resulting 1-methylbenzimidazole is then subjected to a chloromethylation reaction. Chloromethylation reagents are generally used, such as chloromethyl ether or a mixture of triformaldehyde and hydrogen chloride. In a suitable organic solvent, such as dichloromethane or chloroform, 1-methylbenzimidazole is mixed with a chloromethylation reagent and reacted at low temperature to room temperature, usually 0 - 25 ° C, for several hours. In this process, chloromethyl replaces hydrogen atoms at specific locations on the benzimidazole ring, resulting in 2 - (chloromethyl) - 1 - methyl - 1H - benzo [d] imidazole. After the
    reaction is completed, the product is treated by conventional separation and purification methods, such as extraction, distillation, recrystallization, etc., to obtain a high-purity target product. The entire synthesis process requires strict control of reaction conditions, including temperature, time, raw material ratio, etc., to ensure the smooth progress of the reaction and the good yield and purity of the product.
    In which fields is 2- (chloromethyl) -1-methyl-1H-benzo [d] imidazole used?
    2-%28chloromethyl%29-1-methyl-1H-benzo%5Bd%5Dimidazole, Chinese name 2- (chloromethyl) -1 -methyl-1H-benzo [d] imidazole, this substance has a wide range of uses.
    In the field of medicine, it is often a key intermediate for the synthesis of new drugs. Because of its special chemical structure, it can interact with many targets in organisms, helping to develop antibacterial and antiviral drugs. For example, by modifying the structure of this compound, drugs with high selective inhibitory activity against specific bacteria can be obtained, opening up new avenues for the treatment of infectious diseases.
    In the field of materials science, it can participate in the preparation of functional polymer materials. Added to polymer, it can improve the thermal stability and mechanical properties of materials. For example, it is used in the preparation of high-performance engineering plastics to improve the performance of plastics in high temperature and high pressure environments, making the material more suitable for aerospace, automobile manufacturing and other fields that require strict material properties.
    In the field of organic synthesis, as an important reaction substrate, it participates in the construction of a variety of complex organic compounds. Due to its benzimidazole ring and chloromethyl structure, various reactions such as nucleophilic substitution and cyclization can occur, providing an effective method for the synthesis of organic molecules with specific structures and functions, promoting the development of organic synthesis chemistry, and helping scientists create more novel and unique organic compounds.
    What is the market outlook for 2- (chloromethyl) -1-methyl-1H-benzo [d] imidazole?
    2-%28chloromethyl%29-1-methyl-1H-benzo%5Bd%5Dimidazole is 2 - (chloromethyl) -1 - methyl - 1H - benzo [d] imidazole. The market prospect of this compound needs to be reviewed by many parties.
    From the perspective of demand, this compound has attracted much attention in the field of pharmaceutical chemicals. In pharmaceutical research and development, it may be a key intermediate, which can be used to create new drugs to treat specific diseases. With the growth of the global population, the aging of the population and the improvement of health concerns, the demand for novel active ingredients in the pharmaceutical market is increasing day by day, and the demand for this compound may increase due to its potential value in drug synthesis. In the fine chemical industry, it can be used as a raw material for the synthesis of special functional materials, such as materials with specific optical and electrical properties. With the rapid development of electronics, optics and other industries, the demand for special functional materials will also drive the market demand for this compound.
    From the perspective of supply, its synthesis may have certain difficulties and technical barriers, requiring specific reaction conditions and processes. However, with the continuous advancement of chemical technology, if there are efficient and green synthesis methods emerging, more companies will be encouraged to invest in production and increase market supply. However, in this process, the stability and cost of raw material supply also need to be considered. If the supply of raw materials is limited or the price fluctuations are severe, it will affect its production and market supply.
    Furthermore, the competitive situation also affects its market prospects. If there are few producers of this compound in the market, forming an oligopoly or monopoly pattern, its pricing power and market control will be stronger; if new enterprises continue to pour in, competition intensifies, product prices may be impacted, enterprises need to rely on technology, cost, quality and other advantages to seek development.
    Regulations and policies are also important factors. The chemical and pharmaceutical industries are strictly regulated. If relevant regulations set higher standards for their production, use, environmental protection, etc., enterprises need to invest more resources in compliance, or affect production and marketing activities. On the contrary, if policies encourage innovative drug research and development and the development of fine chemicals, it will bring benefits to them.
    To sum up, the market prospect of 2- (chloromethyl) -1 -methyl-1H-benzo [d] imidazole contains both opportunities and challenges. If it can adapt to market demand, break through technical bottlenecks, cope with competition and comply with regulations and policies, it is expected to achieve good development in the market.