Название продукции:5-Aminomethyl-3H-imidazole-4-carboxylic acid ethyl ester

IUPAC Name:ethyl 4-(aminomethyl)-1H-imidazole-5-carboxylate

CAS:1330764-24-3
Молекулярная формула:C7H11N3O2
Чистота:95%
Номер в каталоге:CM323370
Молекулярная масса:169.18

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Информация о продукции

Номер CAS:1330764-24-3
Молекулярная формула:C7H11N3O2
Точка плавления:-
Smiles-код:O=C(C1=C(CN)N=CN1)OCC
Плотность:
Номер в каталоге:CM323370
Молекулярная масса:169.18
Точка кипения:
Номер Mdl:MFCD20230573
Хранение:

Category Infos

Imidazoles
Imidazole is an important five-membered nitrogen-containing heterocyclic compound. Among the numerous heterocyclic compounds, imidazole and its derivatives are regarded as a unique and multifaceted scaffold material due to their diverse applications in industrial, organic and pharmaceutical chemistry. Imidazoles interact in different ways with many therapeutic targets, enzymes and receptors in biological systems and thus exhibit a wide range of biological activities. In particular, several imidazoles can be used as clinical drugs to treat various types of cancer with high therapeutic efficacy. Furthermore, imidazoles are one of the most critical segments in the field of anti-covid-19 virus drug discovery due to their ability to interact with active targets in living systems.
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Product Other Information

Product Overview 5-Aminomethyl-3H-imidazole-4-carboxylic acid ethyl ester (AMICE) is a widely used reagent in the chemical industry for synthesizing a wide range of compounds. It is an important intermediate in the synthesis of pharmaceuticals, agricultural chemicals, and other organic and inorganic compounds. AMICE is a versatile reagent that is widely used in organic chemistry, biochemistry, and medicinal chemistry.
Synthesis and Application 5-Aminomethyl-3H-imidazole-4-carboxylic acid ethyl ester can be synthesized using a variety of methods. The most common method is the reaction of ethyl chloroformate with an amine in the presence of a base, such as sodium hydroxide. The reaction produces ethyl ester of the carboxylic acid. This can then be reacted with a secondary amine, such as aniline, to produce 5-Aminomethyl-3H-imidazole-4-carboxylic acid ethyl ester. Other methods of synthesis include the reaction of ethyl chloroformate with an amine in the presence of a Lewis acid, such as boron trifluoride, or the reaction of ethyl chloroformate with an amine in the presence of a Grignard reagent, such as magnesium chloride. 5-Aminomethyl-3H-imidazole-4-carboxylic acid ethyl ester has a wide range of applications in scientific research. It has been used in the synthesis of novel compounds for medicinal chemistry, biochemistry, and organic chemistry. It has also been used in the synthesis of polymers for drug delivery, in the synthesis of fluorescent probes for imaging, and in the synthesis of enzyme inhibitors.
Future Directions There are many potential future directions for the use of 5-Aminomethyl-3H-imidazole-4-carboxylic acid ethyl ester. It could be used in the synthesis of novel compounds for drug discovery, or in the synthesis of polymers for drug delivery. It could also be used in the synthesis of fluorescent probes for imaging or enzyme inhibitors. Additionally, further research into its biochemical and physiological effects could provide new insights into its potential therapeutic uses. Finally, further research into its stability and shelf-life could lead to improved methods for its storage and use.