1 Methyl 1h Imidazole 4 Carboxylic Acid Methyl Ester
quinoline thiophene imidazole thiazole

1-methyl-1h-imidazole-4-carboxylic acid methyl ester

    Specifications

    HS Code

    284004

    Name 1-methyl-1H-imidazole-4-carboxylic acid methyl ester
    Molecular Formula C6H8N2O2
    Molecular Weight 140.14
    Appearance Typically a solid or liquid (no standard color specified without more data)
    Melting Point No standard value provided without more data
    Boiling Point No standard value provided without more data
    Density No standard value provided without more data
    Solubility Solubility details vary by solvent, no general data provided
    Pka No standard value provided without more data
    Flash Point No standard value provided without more data

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    General Information
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    Frequently Asked Questions

    As a leading 1-methyl-1h-imidazole-4-carboxylic acid methyl ester 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 1-methyl-1h-imidazole-4-carboxylic acid methyl ester
    1-Methyl-1H-imidazole-4-carboxylic acid methyl ester, this is an organic compound. Looking at its structure, it contains an imidazole ring, with a methyl group at 1 position and a methyl group at 4 positions.
    It has many chemical properties. Because it contains an ester group, it can undergo hydrolysis. Under the catalysis of acid or base, the ester group is hydrolyzed, and when catalyzed by acid, 1-methyl-1H-imidazole-4-carboxylic acid and methanol are formed; when catalyzed by base, the corresponding carboxylate and methanol are obtained. < Br >
    Because it contains an imidazole ring, the nitrogen atom has a solitary pair of electrons, which is alkaline and can react with acids to form salts. At the same time, the imidazole ring is aromatic and relatively stable, and can participate in electrophilic substitution reactions, such as halogenation, nitrification, etc. The substitution check point is mostly at the higher active position of the imidazole ring.
    The solubility of this compound also needs attention. Generally, it has a certain solubility in organic solvents such as dichloromethane, chloroform, ethanol, etc., but its solubility in water may be limited. Because of its structure, the hydrophobic part accounts for a large proportion. < Br >
    Its chemical properties make it widely used in the field of organic synthesis, and can be used as a key intermediate to construct more complex organic molecular structures through a series of reactions. It has potential value in the fields of medicinal chemistry, materials science, and other fields.
    What are the synthesis methods of 1-methyl-1h-imidazole-4-carboxylic acid methyl ester
    The synthesis method of methyl 1-methyl-1H-imidazole-4-carboxylic acid has been known for a long time. In the past, many parties followed the classical organic synthesis path.
    First, based on 1-methyl-1H-imidazole-4-carboxylic acid, it was co-placed in a reactor with methanol, supplemented by concentrated sulfuric acid as a catalyst, heated to a suitable degree, and the esterification reaction was carried out. At that time, it was necessary to strictly control the temperature and reaction time to make the two fully blend and esterification occurred. After separation and purification, this ester could be obtained.
    Second, there are also those who use the corresponding halogenate as the starting material. First, a suitable halogenated imidazole derivative is taken, interacted with a nucleophilic reagent such as sodium methoxide, and through the reaction of nucleophilic substitution, a methoxy group is introduced to generate the target product. In this way, the selection of halogenate, the amount of nucleophilic reagent and the control of reaction conditions are all key.
    Third, there are still those who are post-esterified through the construction of imidazole rings. First, the imidazole ring is formed by cyclization reaction with suitable nitrogen-containing and carbon-containing raw materials, and then it is methylated. Then, under esterification conditions, an appropriate carboxylic acid derivative is used to generate 1-methyl-1H-imidazole-4-carboxylic acid methyl ester. There are many steps in this process, but each step requires fine operation to obtain a pure product.
    All this synthesis method has advantages and disadvantages. Although the classic esterification method is relatively simple to operate, the corrosiveness of the catalyst and the difficulty of product separation are also insufficient. Nucleophilic substitution of halogenated compounds requires strict requirements on the purity of raw materials and reaction conditions. Although the molecular structure can be designed according to the needs of the imidazole ring, the steps are complicated and time-consuming. All parties need to choose the appropriate method according to the purity of their own raw materials, equipment and products.
    What is the use of 1-methyl-1h-imidazole-4-carboxylic acid methyl ester
    1-Methyl-1H-imidazole-4-carboxylic acid methyl ester, which has a wide range of uses. In the field of medicinal chemistry, it is often used as a key intermediate. Taking the synthesis of specific drug molecules as an example, with its unique chemical structure, it can participate in many types of reactions and build a specific chemical skeleton required for drug activity, which is of great significance in the process of new drug development.
    In the field of materials science, it also has important applications. Or it can be integrated into polymer materials through specific reaction paths, giving materials unique properties, such as improving material thermal stability and mechanical properties, providing new possibilities for the preparation of high-performance functional materials.
    In addition, in the field of organic synthesis, methyl 1-methyl-1H-imidazole-4-carboxylate is often used as a reactant in the synthesis of complex organic compounds due to its active chemical properties. Through ingenious design of reaction routes, many special structural organic molecules can be constructed, injecting vitality into the development of organic synthesis chemistry, and making significant contributions to enriching the variety of organic compounds and expanding organic synthesis methods.
    1-methyl-1h-imidazole-4-carboxylic acid methyl ester market prospects
    1-Methyl-1H-imidazole-4-carboxylic acid methyl ester, this product has considerable market prospects at present.
    In the Guanfu chemical industry, this compound is often the backbone raw material for organic synthesis. Its unique chemical structure gives the possibility of many reactions and can be used to prepare many high-value-added fine chemicals. Today, the field of pharmaceutical research and development is booming, and there is an increasing demand for novel and efficient intermediates. 1-Methyl-1H-imidazole-4-carboxylic acid methyl ester, with its characteristics, often plays a key role in the process of creating new drug molecular structures, so the demand for it in the pharmaceutical industry is on the rise.
    Furthermore, it is also favored in the field of materials science. With the in-depth research of functional materials, materials derived from this compound have shown unique advantages in optical and electrical properties, and may be applied to emerging fields such as optoelectronic devices and sensors, expanding the boundaries of their market applications.
    However, there are also challenges in the market. Its synthesis process needs to be continuously refined to reduce costs and increase productivity. And the chemical industry is fiercely competitive, with new entrants and incumbents competing for market share. However, overall, with the advancement of science and technology, the demand for 1-methyl-1H-imidazole-4-carboxylic acid methyl ester in various related fields is expected to continue to grow, and the market prospect is bright. Over time, it may occupy a more important position in the chemical industry chain, injecting strong impetus into the development of the industry.
    1-methyl-1h-imidazole-4-carboxylic acid methyl ester in storage and transportation
    Methyl 1-methyl-1H-imidazole-4-carboxylate is an organic compound. When storing and transporting, there are many key considerations that need to be paid attention to.
    When storing, the first environment should be selected. It should be placed in a cool, dry and well-ventilated place. This is because if the compound is heated or causes internal structural changes, it will affect its chemical properties. Humid environments can easily lead to reactions such as hydrolysis, so it is essential to keep it dry.
    Furthermore, it is necessary to keep away from fires and heat sources. Because of its flammability, it can be exposed to open flames, hot topics or cause combustion, and even explosions, endangering the safety of personnel and facilities.
    At the same time, it should be stored separately from oxidants, acids, alkalis, etc. Due to the chemical reaction of these substances with 1-methyl-1H-imidazole-4-carboxylic acid methyl ester, or the release of a large amount of heat, or the formation of harmful products, resulting in accidents.
    In terms of transportation, the packaging must be tight. Choose suitable packaging materials to prevent leakage during transportation. Choose sturdy containers and take protective measures to avoid package damage caused by collisions and vibrations.
    During transportation, relevant regulations must also be strictly followed. Transportation vehicles need to be equipped with corresponding fire equipment and leakage emergency treatment equipment. In the event of an accident, they can be responded to in time.
    In addition, transportation personnel should also be familiar with the characteristics of the compound and emergency treatment methods. In case of leakage and other situations, effective measures can be taken quickly to reduce the harm.
    In short, the storage and transportation of 1-methyl-1H-imidazole-4-carboxylic acid methyl ester is related to safety and quality, and it is necessary to strictly follow the specifications to ensure that all links are correct.