1h Benzimidazole 2 Carboxylic Acid 4 Methyl
quinoline thiophene imidazole thiazole

1H-benzimidazole-2-carboxylic acid, 4-methyl-

    Specifications

    HS Code

    428898

    Chemical Formula C9H8N2O2
    Molar Mass 176.17 g/mol
    Appearance Solid (usually powder)
    Melting Point Data may vary, typically in a certain range
    Solubility In Water Low solubility
    Solubility In Organic Solvents May dissolve in some organic solvents like DMSO
    Pka Value Related to its acidic nature, specific value depends on conditions
    Density Data may be available in literature for specific forms
    Crystal Structure Specific crystal structure details can be determined by X - ray diffraction

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    1H - benzimidazole - 2 - carboxylic acid, 4 - methyl - what are the chemical properties
    4-Methyl-1H-benzimidazole-2-carboxylic acid, this is an organic compound. It has unique chemical properties.
    When it comes to physical properties, it is mostly solid at room temperature, and the melting and boiling point varies depending on the force between molecules. There are benzimidazole rings and carboxyl groups in the molecule. The benzimidazole ring has a certain rigidity and conjugation system, so that the substance has specific stability and electron cloud distribution. The existence of carboxyl groups gives it a certain polarity, or affects its solubility in different solvents. It may have a certain solubility in polar solvents such as water, because carboxyl groups can form hydrogen bonds with water molecules.
    In terms of chemical properties, the carboxyl group is acidic and can be neutralized with bases to form corresponding carboxylic salts. This property can be used in organic synthesis to prepare derivatives or regulate the pH of reaction systems. At the same time, the nitrogen atom on the benzimidazole ring has lone pairs of electrons, which can participate in the reaction as an electron donor, such as coordination with metal ions to form metal complexes. Such complexes may have unique applications in catalysis and materials science.
    In addition, 4-methyl substituents also have an impact on molecular properties. Methyl is the power supply group, which can increase the electron cloud density of the benzimidazole ring through induction effects, affect the activity of electrophilic substitution reactions on the ring, or make the reaction more prone to occur in specific locations. Its steric hindrance effect may change the molecular spatial configuration, affect the interaction between molecules, and have an effect on its aggregate state and crystal structure.
    What is the main use of 1H - benzimidazole - 2 - carboxylic acid, 4 - methyl -
    1H-benzimidazole-2-carboxylic acid, 4-methyl, this is an organic compound. It has a wide range of uses in the field of medicine and is often a key intermediate in drug synthesis. The structure of Geinbenzimidazole has a variety of biological activities and can be chemically modified to meet the needs of specific drug targets, such as the development of some antibacterial, antiviral and anti-tumor drugs.
    It is also useful in the field of materials science. It can be introduced into polymer materials through chemical reactions to improve the properties of materials, such as improving the stability and thermal properties of materials. Due to its special molecular structure, it may endow materials with unique physical and chemical properties, meeting the special requirements of materials in different fields.
    In the field of pesticides, it can also be seen. Or it can be used as an important part of pesticide active ingredients, used to synthesize pesticide products with insecticidal, bactericidal or herbicidal effects, and contribute to agricultural pest control and weed control. In short, although 1H-benzimidazole-2-carboxylic acid, 4-methyl is an organic compound, it plays an important role in many fields such as medicine, materials, and pesticides, and is of great significance to promote the development of various fields.
    What are the synthesis methods of 1H - benzimidazole - 2 - carboxylic acid, 4 - methyl -
    There are many ways to synthesize 4-methyl-1H-benzimidazole-2-carboxylic acid.
    First, phthalamine and 4-methyl-ethyl formate are used as starting materials. First, phthalamine and 4-methyl-ethyl formate are mixed in a suitable solvent, such as ethanol or toluene. Under the condition of heating and reflux, the two condensation reactions occur. During this process, the amino group of phthalamine interacts with the ester group of 4-methyl-ethyl formate to remove the ethanol molecule and gradually form 4-methyl-1H-benzimidazole-2-carboxylate ethyl ester. Subsequently, the resulting ester product is treated with alkali solution such as sodium hydroxide, and the ester group is hydrolyzed into a carboxyl group in the environment of hydrolysis, and then the target product 4-methyl-1H-benzimidazole-2-carboxylic acid is obtained. Finally, the purified product can be obtained through acidification, separation and purification.
    Second, o-nitroaniline is used as the starting material. First, the reduction reaction of o-nitroaniline is carried out, and the nitro group is reduced to an amino group with iron powder and hydrochloric acid as the reducing agent to obtain o-phenylenediamine. Then, as in the first method above, the o-phenylenediamine is condensed with 4-methyl-ethyl formate, and then hydrolyzed and acidified to finally synthesize 4-methyl-1H-benzimidazole-2-carboxylic acid.
    Third, 2-aminobenzimidazole is used as raw material. It is methylated first, and a suitable methylation reagent is selected, such as iodomethane or dimethyl sulfate. Under basic conditions, such as the presence of potassium carbonate, the nitrogen atom of 2-aminobenzimidazole is methylated to form 4-methyl-2-aminobenzimidazole. Then, by suitable oxidation reagents, such as potassium permanganate or potassium dichromate, it is oxidized to convert the amino group into a carboxyl group, thereby obtaining 4-methyl-1H-benzimidazole-2-carboxylic acid. After the reaction, high-purity products are obtained through separation, purification, and other operations.
    1H - benzimidazole - 2 - carboxylic acid, 4 - methyl - in which areas
    4-Methyl-1H-benzimidazole-2-carboxylic acid, which is useful in many fields. In the field of medicine, because of its unique chemical structure, or potential biological activity, it can help to create new drugs. Doctors say: "The miraculous effect of medicine comes from the delicacy of matter." This compound may act on specific biological targets, regulate physiological processes, and is expected to become a good medicine for treating diseases.
    In the field of materials science, it can be used as the basis for building new functional materials. Using it as a raw material, through ingenious craftsmanship, or materials with special properties can be made, such as those with the ability to identify and absorb specific substances, should be "ingenious, make the best use of things". < Br >
    In the field of organic synthesis, it is a key intermediate. Organic synthesizers can use it to introduce specific structures and expand molecular diversity, such as building complex ring structures, just like skilled craftsmen building exquisite pavilions, enriching the types of organic compounds, opening up new avenues for scientific research and industrial production.
    1H - benzimidazole - 2 - carboxylic acid, 4 - methyl - What is the market outlook?
    4-Methyl-1H-benzimidazole-2-carboxylic acid, this is a class of organic compounds. Looking at its market prospects, it has a great development trend.
    In the field of medicine, it has emerged. Many studies have shown that such compounds contain specific structures and can interact with targets in vivo. For example, specific proteins specific to certain tumor cells can be accurately identified and bound, or may become a key raw material for the development of new anti-cancer drugs. With the increasing incidence of cancer, the demand for anti-cancer drugs is increasing, and 4-methyl-1H-benzimidazole-2-carboxylic acid is expected to continue to grow as a potential drug intermediate.
    In the field of materials science, it also has potential. Due to its unique electrical and optical properties, it can be applied to organic Light Emitting Diode (OLED) materials. OLED displays are popular in mobile phones, TVs and other display fields due to their advantages of self-luminous, wide viewing angle and fast response speed. If 4-methyl-1H-benzimidazole-2-carboxylic acid can contribute to the improvement of OLED material properties, it will definitely open up a broad market space.
    Furthermore, in the field of agriculture, it may become the basis for the development of new pesticides. Some structural compounds containing benzimidazole have good control effects on crop diseases and insect pests, and 4-methyl-1H-benzimidazole-2-carboxylic acid may be derived from highly efficient, low-toxic and environmentally friendly pesticide products. With the deepening of people's attention to food safety and environmental protection, the market demand for such new pesticides will also gradually rise.
    However, its market development also poses challenges. The complexity of the synthesis process makes the production cost high and restricts large-scale application. And the market competition is fierce, many scientific research institutions and enterprises are committed to similar or alternative Product Research & Development. To stand out in the market, it is necessary to continuously optimize the synthesis process, reduce costs, and improve product quality and performance.