1 Methyl 1h Imidazole 4 5 Dicarboxylic Acid
Quinoline Thiophene Imidazole Thiazole
1-methyl-1H-imidazole-4,5-dicarboxylic acid
Name 1-methyl-1H-imidazole-4,5-dicarboxylic acid
Chemical Formula C6H6N2O4
Molar Mass 170.12 g/mol
Appearance Solid (description may vary)
Solubility Solubility characteristics in different solvents would need further research
Melting Point Specific melting point data requires literature search
Density Density data would need experimental determination or literature lookup
Stability Stability under various conditions (light, heat, etc.) needs research
FAQ

1-methyl-1H-imidazole-4, what are the chemical properties of 5-dicarboxylic acid

1 - methyl - 1H - imidazole - 4,5 - dicarboxylic acid, Chinese name 1 - methyl - 1H - imidazole - 4,5 - dicarboxylic acid, this is an organic compound with unique chemical properties.

Looking at its structure, it is significantly acidic because it contains carboxyl groups (-COOH) and imidazole rings. The carboxyl group can ionize hydrogen ions, exhibit acidic properties in aqueous solution, and can neutralize with bases to generate corresponding salts and water.

The compound has two carboxyl groups and can participate in esterification reactions under suitable conditions. Alcohols are co-heated with them. Under the action of a catalyst, the hydroxyl group in the carboxyl group combines with the hydrogen atom in the alcohol to form water, and then forms an ester compound. This reaction is often used in organic synthesis to prepare specific ester products.

Its imidazole ring structure endows the molecule with certain stability and reactivity. The nitrogen atom in the imidazole ring has a lone pair of electrons, which can be used as an electron donor to participate in the coordination reaction and form complexes with metal ions. This property is of great significance in the fields of materials science and bioinorganic chemistry, such as potential applications in the design of new metal complex catalysts.

At the same time, 1-methyl-1H-imidazole-4,5-dicarboxylic acid may also participate in nucleophilic substitution reactions. The presence of carboxyl groups makes the carbon atoms connected to them partially positively charged, vulnerable to attack by nucleophiles, resulting in substitution reactions, providing the possibility for the construction of more complex organic molecular structures.

In summary, 1-methyl-1H-imidazole-4,5-dicarboxylic acid has shown important chemical properties and potential application value in many fields such as organic synthesis and coordination chemistry due to its unique structure.

1-methyl-1H-imidazole-4, what are the common uses of 5-dicarboxylic acid

1 - methyl - 1H - imidazole - 4,5 - dicarboxylic acid is 1 - methyl - 1H - imidazole - 4,5 - dicarboxylic acid, which is an organic compound with a wide range of uses in chemical synthesis and pharmaceutical research and development. Common uses are as follows:
First, the key intermediate in organic synthesis. Because its molecule contains imidazole ring and carboxylic group, it can derive many compounds with unique properties and uses through various chemical reactions, such as esterification, amidation, etc. In the field of medicinal chemistry, new drug molecules can be created by modifying their structure. For example, amidation with specific amine compounds can prepare amide derivatives with potential biological activities, or be used in the development of anti-cancer and anti-inflammatory drugs.
Second, ligands for metal complexes. With the nitrogen atom of carboxyl and imidazole rings, the compound can coordinate with a variety of metal ions to construct rich metal complexes. These complexes exhibit unique properties in the fields of catalysis and materials science. For example, complexes formed with transition metal ions can be used as high-efficiency catalysts for organic synthesis reactions to improve reaction efficiency and selectivity; in the field of materials science, functional materials with special optical and electrical properties can be prepared.
Third, in the field of medicine, or have certain biological activities. Studies have shown that some imidazole derivatives have antibacterial, antiviral, anti-tumor and other biological activities. 1-methyl-1H-imidazole-4,5-dicarboxylic acid may be structurally optimized to develop drugs with specific therapeutic effects. For example, some of its derivatives may play an anti-tumor role by modulating specific signaling pathways in the organism.

1-methyl-1H-imidazole-4, what is the synthesis method of 5-dicarboxylic acid

1 - methyl - 1H - imidazole - 4,5 - dicarboxylic acid is 1 - methyl - 1H - imidazole - 4,5 - dicarboxylic acid, which can be synthesized as follows:

can be prepared from suitable starting materials through a multi-step reaction. First take an imidazole compound with a suitable substituent, and under specific reaction conditions, react with a methylating agent to introduce methyl groups. Commonly used methylation reagents, such as iodomethane, react with imidazole compounds under the catalysis of bases. Potassium carbonate can be selected for the base, etc., in a suitable organic solvent, such as N, N-dimethylformamide (DMF), heated and stirred to achieve methylation at the 1-position.

Subsequently, the methylated imidazole derivatives are carboxylated. Carbon dioxide can be used as the carboxyl source, and the carboxylation at the 4,5-position can be achieved under the action of metal catalysts, such as palladium catalysts, under specific solvent, reaction temperature and pressure conditions. For example, in a certain pressure of carbon dioxide atmosphere, with an appropriate amount of palladium catalyst and ligand, in a suitable solvent such as tetrahydrofuran (THF), the reaction is heated for a certain period of time, so that the carboxyl group is introduced at the 4,5-position to obtain 1-methyl-1H-imidazole-4,5-dicarboxylic acid.

During the reaction process, the reaction conditions, such as temperature, time, and reagent dosage, need to be carefully adjusted to ensure the efficient progress of the reaction and the high purity of the product. After each step of the reaction, it is often necessary to use methods such as column chromatography and recrystallization to separate and purify the product to obtain a pure intermediate product and the final target product 1-methyl-1H-imidazole-4,5-dicarboxylic acid.

1-methyl-1H-imidazole-4, in which areas is 5-dicarboxylic acid used?

1 - methyl - 1H - imidazole - 4,5 - dicarboxylic acid, that is, 1 - methyl - 1H - imidazole - 4,5 - dicarboxylic acid, this compound has applications in many fields.

In the field of pharmaceutical research and development, it shows unique efficacy. Because its structure contains specific functional groups, it can precisely bind to targets in organisms. By modifying its structure, new drugs can be created. For example, it can be developed as an anti-cancer drug, which inhibits the growth and spread of cancer cells by interfering with specific metabolic pathways of cancer cells; or as an antibacterial drug, which destroys bacterial cell walls or cell membranes, for the purpose of antibacterial.

In the field of materials science, 1-methyl-1H-imidazole-4,5-dicarboxylic acid also has important uses. It can be used as a ligand to complex with metal ions to prepare metal-organic framework materials (MOFs). Such materials have high specific surface area and regular pore structure, and perform well in the field of gas adsorption and separation. For example, they can efficiently absorb carbon dioxide and help to solve the problem of greenhouse gas emission reduction. In the field of catalysis, MOFs materials can catalyze many organic reactions with their unique structure and activity check point, improving reaction efficiency and selectivity.

In the field of chemical synthesis, 1-methyl-1H-imidazole-4,5-dicarboxylic acid can be used as a key intermediate. Using the activity of its two carboxyl groups and methyl imidazole ring, through esterification, amidation and other reactions, organic compounds with more complex structures and diverse functions can be synthesized, providing a rich material basis for the development of organic synthetic chemistry.

1-methyl-1H-imidazole-4, what is the market prospect of 5-dicarboxylic acid?

1-Methyl-1H-imidazole-4,5-dicarboxylic acid, this product has a promising future in the current market. Looking at its characteristics, it is a key raw material for organic synthesis and has a wide range of uses. In the field of medicine, it can lay the foundation for the creation of new drugs, help develop effective prescriptions, and cure many diseases. Therefore, in the pharmaceutical industry, demand is expected to rise steadily. In the field of materials science, it can be used to prepare functional materials with excellent performance. It plays a unique role in cutting-edge fields such as electronics and optics, prompting related industries to pay more and more attention to it.

Furthermore, with the advance of scientific research, the exploration and research of its derivatives continue to deepen. The emergence of new synthesis methods has made it possible for production costs to decrease, thereby enhancing their market competitiveness. Coupled with the increasing popularity of environmental protection concepts, if a breakthrough can be made on the green synthesis path, it will be able to meet the market demand for sustainable materials and further expand the market space.

However, the road to the market is not smooth. Competition in the same industry may become increasingly fierce, and new entrants may use various means to gain share. And fluctuations in raw material prices will also affect their costs and profits. Only by understanding market dynamics, constantly innovating production processes, and improving product quality can we stand at the forefront of the market wave and enjoy the dividends brought by the broad prospects.