Ethyl 4-methyl-2-(methylamino)-1,3-thiazole-5-carboxylate, with the CAS number 3161-68-0, is a chemical compound that belongs to the thiazole family, characterized by a five-membered ring containing sulfur and nitrogen atoms. This compound features an ethyl ester functional group, which contributes to its solubility in organic solvents. The presence of a methylamino group enhances its potential for biological activity, making it of interest in medicinal chemistry. The thiazole ring is known for its role in various pharmacological applications, including antimicrobial and anti-inflammatory properties. The compound's structure suggests it may participate in various chemical reactions, such as nucleophilic substitutions or condensation reactions, due to the reactivity of the carboxylate and amino groups. Its physical properties, such as melting point, boiling point, and solubility, would typically depend on the specific conditions and purity of the sample. Overall, this compound's unique structure and functional groups make it a subject of interest for further research in chemical and pharmaceutical applications.

ethyl 4-methyl-2-(methylamino)-1,3-thiazole-5-carboxylate

3161-68-0: Ethyl 4-methyl-2-(methylamino)-1,3-thiazole-5-carboxylate, with the CAS number 3161-68-0, is a chemical compound that belongs to the thiazole family, characterized by a five-membered ring containing sulfur and nitrogen atoms. This compound features an ethyl ester functional group, which contributes to its solubility in organic solvents. The presence of a methylamino group enhances its potential for biological activity, making it of interest in medicinal chemistry. The thiazole ring is known for its role in various pharmacological applications, including antimicrobial and anti-inflammatory properties. The compound's structure suggests it may participate in various chemical reactions, such as nucleophilic substitutions or condensation reactions, due to the reactivity of the carboxylate and amino groups. Its physical properties, such as melting point, boiling point, and solubility, would typically depend on the specific conditions and purity of the sample. Overall, this compound's unique structure and functional groups make it a subject of interest for further research in chemical and pharmaceutical applications.

CAS 3161-68-0

ethyl 4-methyl-2-(methylamino)-1,3-thiazole-5-carboxylate

Ethyl 4-methyl-2-(methylamino)thiazole-5-carboxylate

Ref: IN-DA00CLUQ

Ethyl 4-methyl-2-(methylamino)thiazole-5-carboxylate

Ref: 54-OR1063170

Ethyl 4-methyl-2-(methylamino)thiazole-5-carboxylate

Ref: 10-F788104