Methyl 2 Ethoxy 3h Benzimidazole 4 Carboxylate
quinoline thiophene imidazole thiazole

methyl 2-ethoxy-3H-benzimidazole-4-carboxylate

    Specifications

    HS Code

    822408

    Chemical Formula C12H14N2O3
    Molecular Weight 234.25
    Appearance Solid (usually)
    Physical State At Room Temperature Solid
    Odor Typically odorless or faint odor
    Melting Point Data may vary, needs experimental determination
    Boiling Point Data may vary, needs experimental determination
    Solubility In Water Low solubility
    Solubility In Organic Solvents Moderate solubility in some organic solvents like ethanol, dichloromethane
    Stability Stable under normal conditions
    Ph Neutral (in solution, depends on medium)
    Color May be white to off - white

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    Frequently Asked Questions

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    What is the chemical structure of methyl 2-ethoxy-3H-benzimidazole-4-carboxylate?
    Methyl-2-ethoxy-3H-benzimidazole-4-carboxylic acid ester, its chemical structure is based on a benzimidazole ring system. The benzimidazole ring is fused from a benzene ring and an imidazole ring. In this ring system, the nitrogen atom is in a specific position, giving it unique electronic characteristics and reactivity.
    In this compound, an ethoxy group is connected at the 2nd position of the benzimidazole ring. The ethoxy group is composed of an ethyl group connected to an oxygen atom. Ethyl is a saturated hydrocarbon group with certain hydrophobicity, and the presence of oxygen atoms can affect the polarity of the molecule and the distribution of electron clouds.
    In addition, there is a carboxylic acid methyl ester group at position 4 of the benzimidazole ring, that is, the -COOCH group. In this ester structure, the carbonyl group (C = O) has strong electron-absorbing properties, which will affect the electron cloud density of the surrounding atoms, while the methoxy group (-OCH) contributes to the stability and physicochemical properties of the molecule. Overall, the chemical structure of methyl-2-ethoxy-3H-benzimidazole-4-carboxylate combines the activity of the benzimidazole ring, the hydrophobicity of the ethoxy group, and the characteristics of the carboxylic acid methyl ester group. These structural characteristics together determine the unique properties and potential applications of this compound in many fields such as organic synthesis and medicinal chemistry.
    What are the main uses of methyl 2-ethoxy-3H-benzimidazole-4-carboxylate?
    Methyl-2-ethoxy-3H-benzimidazole-4-carboxylic acid ester, which has a wide range of uses. In the field of medicine, it may be a key raw material for the creation of new drugs. Due to its unique chemical structure, it can interact with specific targets in organisms or regulate physiological functions, and has potential therapeutic effects on certain diseases. For example, when developing targeted drugs for specific diseases, the structural properties of this compound may help to precisely act on diseased cells and achieve therapeutic purposes.
    In the field of materials science, it also has its uses. It can be chemically modified and compounded with other materials to prepare new materials with special properties. Such as improving the stability and mechanical properties of materials, etc., or used to make high-performance polymer materials, used in aerospace, automobile manufacturing and other fields that require strict material properties.
    In the agricultural field, it can be used as a synthetic intermediate of pesticides or plant growth regulators. After rational design and transformation, high-efficiency and low-toxicity pesticides may be developed, which can precisely kill pests and diseases, and have little impact on the environment; or as a plant growth regulator, which regulates the process of plant growth and development, and improves crop yield and quality.
    With its special chemical structure, this compound has shown potential application value in many fields such as medicine, materials, agriculture, etc., providing new opportunities for technological innovation and development in various fields.
    What is the synthesis method of methyl 2-ethoxy-3H-benzimidazole-4-carboxylate?
    The synthesis of methyl 2-ethoxy-3H-benzimidazole-4-carboxylic acid esters is a key research point in the field of chemical synthesis. To make this substance, various paths can be followed.
    First, it can be started from phthalamines and dimethyl ethoxymalonate. Put phthalamines and dimethyl ethoxymalonate in a suitable organic solvent in a specific ratio, such as ethanol, toluene, etc. Then add an appropriate amount of catalysts, such as zinc acetate, p-toluenesulfonic acid, etc., to promote the reaction. Warm up to a certain temperature, usually 80-120 ° C, and continue to stir. In this process, the amino group of o-phenylenediamine and the ester group of dimethyl ethoxymalonate undergo a condensation reaction to form an intermediate first. The intermediate is then cyclized within the molecule to obtain methyl 2-ethoxy-3H-benzimidazole-4-carboxylic acid ester. After the reaction, the product is purified by reduced pressure distillation, column chromatography, etc., and the unreacted raw materials, catalysts and by-products are removed.
    Second, 2-nitroaniline can also be used as the starting material. 2-nitroaniline is first reduced to obtain 2-aminoaniline. Commonly used reducing agents include iron filings-hydrochloric acid, hydrogen-palladium carbon, etc. 2-Aminoaniline and dimethyl ethoxymalonate under reaction conditions similar to the above, through condensation and cyclization, can also obtain the target product methyl 2-ethoxy-3H-benzimidazole-4-carboxylic acid ester. Subsequent purification methods are also needed to improve the purity of the product.
    When synthesizing methyl 2-ethoxy-3H-benzimidazole-4-carboxylic acid esters, the precise control of reaction conditions is crucial, such as temperature, reaction time, raw material ratio, catalyst dosage, etc., all have a significant impact on the reaction yield and product purity. And the purification steps should not be underestimated, which is related to the quality of the final product.
    What are the physical properties of methyl 2-ethoxy-3H-benzimidazole-4-carboxylate?
    Methyl 2-ethoxy-3H-benzimidazole-4-carboxylic acid ester, this is an organic compound. Its physical properties are unique, it is related to many aspects, and it is closely related to practical applications.
    Let's talk about the appearance first. Under normal circumstances, methyl 2-ethoxy-3H-benzimidazole-4-carboxylic acid ester is often white to light yellow crystalline powder. This form is easy to store and transport. During various operations, it is powdery and also conducive to mixing with other substances.
    Besides solubility, this substance exhibits certain solubility in organic solvents such as ethanol and dichloromethane. This property makes it more convenient to participate in various reactions in the field of organic synthesis. It can be used as a reactant or intermediate to dissolve it with a suitable organic solvent, making it easier to interact with other reagents to achieve the desired reaction purpose. However, its poor solubility in water limits its application in aqueous systems. This factor must be taken into account when designing relevant experiments or processes.
    Melting point is also one of its important physical properties. After determination, its melting point is within a certain range, and this melting point data is of great significance for the purity identification of substances. If the melting point of the obtained sample matches the known standard value, it can indicate that the sample is of high purity to a certain extent; if the melting point is deviated, it may suggest that the sample contains impurities and needs to be further purified.
    In addition, methyl 2-ethoxy-3H-benzimidazole-4-carboxylic acid ester also has certain stability. Under conventional temperature and humidity environments, it can maintain its own chemical structure relatively stable. However, when exposed to high temperature, high humidity or a specific chemical environment, its stability may be affected, and then chemical reactions may occur, resulting in chemical structure changes, which requires appropriate measures to be taken according to its stability characteristics during storage and use.
    What is the market outlook for methyl 2-ethoxy-3H-benzimidazole-4-carboxylate?
    Guanfu methyl 2-ethoxy-3H-benzimidazole-4-carboxylic acid ester is worthy of careful investigation in today's market prospects.
    Its potential in the field of scientific research may be extraordinary. Geiin benzimidazole compounds are often the focus of researchers, and many of them have investigated their biological activities and pharmacological properties. Methyl 2-ethoxy-3H-benzimidazole-4-carboxylic acid esters, because of their unique molecular structure, may be able to emerge in the road of drug development. Or it can be used as a lead compound, ingeniously modified and optimized to breed new specific drugs to treat many diseases. This sincerity is a great opportunity, which has attracted countless pharmaceutical companies and scientific research institutions to compete.
    In the field of materials science, it is also possible. Benzimidazole derivatives have unique properties in materials, such as good thermal stability and optical properties. Methyl 2-ethoxy-3H-benzimidazole-4-carboxylic acid esters, or can be treated by special processes, become the key components of new functional materials, and are used in cutting-edge fields such as electronics and optics to open up new frontiers.
    However, its market prospects are not without challenges. The optimization of the synthesis process is a top priority. If the synthesis process is complicated and costly, it is difficult to produce on a large scale, limiting its marketing activities. And in terms of safety and environmental impact, it also needs to be considered in detail. Only by ensuring its safe use and environmental friendliness can it be widely recognized in the market.
    In summary, the market prospect of methyl 2-ethoxy-3H-benzimidazole-4-carboxylic acid ester, opportunities and challenges coexist. If we can overcome the synthesis problem and take into account safety and environmental protection, we will be able to win a place in the market and shine.