Methyl 5 Diethoxymethylimidazole 4 Carboxylate
quinoline thiophene imidazole thiazole

Methyl 5-diethoxymethylimidazole-4-carboxylate

    Specifications

    HS Code

    851193

    Chemical Formula C11H18N2O5
    Molecular Weight 258.27
    Appearance Typically a solid (description may vary based on purity and conditions)
    Melting Point Data might vary, needs experimental determination
    Solubility In Water Limited solubility, likely hydrophobic due to structure
    Solubility In Organic Solvents Soluble in common organic solvents like ethanol, dichloromethane
    Pka Relevant acidic/basic groups' pKa values need experimental determination
    Stability Stable under normal conditions, but may react with strong oxidizing or reducing agents

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    Frequently Asked Questions

    As a leading Methyl 5-diethoxymethylimidazole-4-carboxylate supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    What is Methyl 5-diethoxymethylimidazole-4-carboxylate?
    Methyl-5-diethoxymethylimidazole-4-carboxylic acid ester has a wide range of uses. In the field of medicine, it can be used as a key raw material of traditional Chinese medicine to synthesize various special drugs, such as drugs that have significant curative effects on specific inflammation and tumor diseases. According to ancient methods, when processing various drugs, it can help the drug more easily enter the meridians and make the drug effect more significant.
    In the chemical industry, this substance is also important. It can be used as an intermediate in organic synthesis and transformed into various chemical products with unique functions through a series of delicate reactions. When synthesizing polymer materials with special properties, it can endow the material with special chemical stability and mechanical properties, just like the ancient craftsmen gave the utensils a different character with unique skills.
    Furthermore, in the process of scientific research and exploration, methyl-5-diethoxymethylimidazole-4-carboxylate is also an important research object. By exploring its reaction mechanism and properties, researchers can open up new synthesis paths and application fields, just like the ancients explored novel techniques in the unknown to expand the boundaries of cognition. In the development of new catalysts, it may inspire new ideas, just as the ancients occasionally obtained new formulas in the process of alchemy and pharmaceuticals, contributing to the progress of science and technology.
    What are the synthetic methods of Methyl 5-diethoxymethylimidazole-4-carboxylate?
    The synthesis method of methyl-5-diethoxymethylimidazole-4-carboxylic acid ester, let me tell you in detail.
    To synthesize this product, one method is to use a compound containing imidazole structure as the starting material. First, the specific position of the imidazole is substituted with the reagent containing diethoxy methyl. This reaction requires careful control of the reaction conditions, such as temperature, reaction duration and proportion of the reactants. Usually, it can be carried out in organic solvents, such as toluene, dichloromethane, etc., to ensure sufficient contact of the reactants and the smooth progress of the reaction. The reaction temperature may need to be maintained within a certain range, or between room temperature and moderate heating, depending on the reactant activity.
    Furthermore, carboxylic acid esters can also be used for conversion. First, the carboxylic acid is properly protected, and then a diethoxy methyl group is introduced, and then an imidazole ring is constructed through a series of reactions. In this process, the selection of the protective group is crucial, which must be able to effectively protect the carboxylic acid group and be easy to remove after the subsequent reaction.
    Another approach can be to design a multi-step reaction route, using a combination of different reaction types. For example, some key structural fragments are introduced by nucleophilic substitution reaction, and then an imidazole ring is formed by cyclization reaction. At the same time, diethoxy methyl and carboxylic acid ester groups are introduced in appropriate steps. Each step of the reaction requires fine operation, purification and identification of the reaction product to ensure that the reaction proceeds in the desired direction, and finally obtain methyl-5-diethoxy methylimidazole-4-carboxylate. The synthesis method requires flexible adjustment of the reaction conditions and routes according to the actual situation in order to achieve the preparation of the target product smoothly.
    What are the physical properties of Methyl 5-diethoxymethylimidazole-4-carboxylate?
    Methyl-5-diethoxymethylimidazole-4-carboxylic acid ester is an important compound in organic chemistry. Its physical properties are unique, which is related to the application and characteristics of this compound.
    Looking at its properties, at room temperature, it is mostly in the solid form, due to the intermolecular forces. In the molecular structure, the imidazole ring interacts with the ester group and the diethoxy methyl group to promote the orderly arrangement of molecules to form a solid state.
    In terms of melting point, the melting point of methyl-5-diethoxymethylimidazole-4-carboxylic acid ester is moderate. This melting point is derived from the balance between the chemical bond energy within the molecule and the intermolecular forces. The conjugated structure of the imidazole ring enhances molecular stability, and the ester group and diethoxy methyl also affect the melting point. The moderate melting point makes the compound easy to control under specific conditions, such as heat treatment, and can accurately grasp its physical state transition.
    In terms of solubility, this compound exhibits a certain solubility in organic solvents. Because the molecule has both polar and non-polar parts, polar ester groups and imidazole rings can interact with polar organic solvents to form hydrogen bonds or dipole-dipole interactions; non-polar bisethoxy methyl groups are soluble with non-polar organic solvents. Common organic solvents, such as ethanol, acetone, etc., can dissolve this compound, but its solubility in water is not good, because the intermolecular forces between water molecules and the compound do not match.
    In terms of volatility, methyl-5-diethoxymethylimidazole-4-carboxylate has low volatility. Its molecular structure is tight, and the intermolecular forces are strong, making it difficult to transform from liquid to gaseous. This property makes the compound more stable during storage and use, and it is not easy to be lost due to volatilization.
    In summary, the physical properties of methyl-5-diethoxymethylimidazole-4-carboxylic acid esters, including solid state properties, moderate melting point, specific solubility, and low volatility, are closely related to their molecular structures and are of great significance for their applications in organic synthesis, materials science, and other fields.
    What are the chemical properties of Methyl 5-diethoxymethylimidazole-4-carboxylate?
    Methyl-5-diethoxymethylimidazole-4-carboxylic acid ester, this is an organic compound. Its physical properties are mostly solid or oily liquids. The melting and boiling point varies depending on the intermolecular force. If the intermolecular force is strong, the melting point and boiling point are high.
    In terms of chemical activity, ester groups (- COOCH) are hydrolytic and can react with water under the catalysis of acids or bases. When exposed to acids, it is slowly hydrolyzed into carboxylic acids and alcohols; when exposed to bases, the hydrolysis is accelerated to form carboxylic salts and alcohols. For example, in sodium hydroxide solution, methyl-5-diethoxy methylimidazole-4-carboxylic acid ester is rapidly hydrolyzed to produce 5-diethoxy methylimidazole-4-carboxylate sodium and methanol.
    Diethoxy methyl moiety, because the oxygen atom of ethoxy (-OCH < CH < CH <) has lone pair electrons, can participate in nucleophilic substitution reactions. When encountering nucleophiles, such as halogen ions (X <), ethoxy groups may be replaced to form new halogen-containing derivatives.
    Imidazole ring moiety, rich in electrons, aromatic, and electrophilic substitution reactions can occur. Due to the large electronegativity of nitrogen atoms, the distribution of electron clouds on the ring is uneven, and specific locations are vulnerable to attack by electrophilic reagents. If under appropriate conditions, brominated reactions can occur with electrophilic reagents such as bromine to generate brominated derivatives.
    In addition, the compound may also participate in coordination reactions. The nitrogen atom on the imidazole ring can be used as a ligand to form complexes with metal ions, showing unique properties and applications.
    What is the price range of Methyl 5-diethoxymethylimidazole-4-carboxylate in the market?
    What is the price of methyl-5-diethoxy methylimidazole-4-carboxylic acid ester in the market? I tried to describe it in the style of ancient Chinese saying in "Tiangong Kaiwu".
    Now looking at this methyl-5-diethoxy methylimidazole-4-carboxylic acid ester, it is difficult to determine the market price. It is subject to various factors to cover the change in its price. First, the price of raw materials is essential. If the raw materials are easy to obtain and the production is abundant, the price may be slightly flat; if the raw materials are rare and difficult to obtain, the price must be high.
    Second, the complexity and simplicity of the production method is also related to its price. If the production method is simple and labor is saved, the cost will be reduced, and the price may be close to the people; if the production is difficult, delicate methods are required, and a huge amount of material resources and manpower is expended, the price will be high.
    Furthermore, the supply and demand of the city also affect its price. If there are many applicants, but there are few producers, the so-called supply is in short supply, and the price will rise; if there is more production but less demand, the supply will exceed the demand, and the price may trend downward.
    According to common sense, in this world, if there is no special situation for this product, the price may be between a few yuan per gram and a few tens of yuan. However, this is only the number of times, and the actual price may vary greatly from time to time, place to place, and city to city. If you want to know the exact price, you should carefully observe the market conditions and ask the businesspeople.