Ethyl 2-(4-chlorophenyl)-4-hydroxy-1,3-thiazole-5-carboxylate is a chemical compound characterized by its thiazole ring, which is a five-membered heterocyclic structure containing sulfur and nitrogen. This compound features a carboxylate ester functional group, which contributes to its reactivity and solubility properties. The presence of a 4-chlorophenyl group enhances its biological activity and may influence its pharmacological properties. The hydroxyl group at the 4-position of the thiazole ring can participate in hydrogen bonding, affecting the compound's interactions with biological targets. Ethyl 2-(4-chlorophenyl)-4-hydroxy-1,3-thiazole-5-carboxylate is often studied for its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals. Its molecular structure suggests potential for various chemical reactions, including esterification and nucleophilic substitutions. Overall, this compound exemplifies the diverse functionalities that can be derived from heterocyclic chemistry, making it a subject of interest in both synthetic and applied chemistry contexts.

ethyl 2-(4-chlorophenyl)-4-hydroxy-1,3-thiazole-5-carboxylate

263016-08-6: Ethyl 2-(4-chlorophenyl)-4-hydroxy-1,3-thiazole-5-carboxylate is a chemical compound characterized by its thiazole ring, which is a five-membered heterocyclic structure containing sulfur and nitrogen. This compound features a carboxylate ester functional group, which contributes to its reactivity and solubility properties. The presence of a 4-chlorophenyl group enhances its biological activity and may influence its pharmacological properties. The hydroxyl group at the 4-position of the thiazole ring can participate in hydrogen bonding, affecting the compound's interactions with biological targets. Ethyl 2-(4-chlorophenyl)-4-hydroxy-1,3-thiazole-5-carboxylate is often studied for its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals. Its molecular structure suggests potential for various chemical reactions, including esterification and nucleophilic substitutions. Overall, this compound exemplifies the diverse functionalities that can be derived from heterocyclic chemistry, making it a subject of interest in both synthetic and applied chemistry contexts.

CAS 263016-08-6

ethyl 2-(4-chlorophenyl)-4-hydroxy-1,3-thiazole-5-carboxylate

Ethyl 2-(4-chlorophenyl)-4-hydroxy-1,3-thiazole-5-carboxylate

Ref: IN-DA002SMC

Ethyl 2-(4-chlorophenyl)-4-hydroxy-1,3-thiazole-5-carboxylate

Ref: 54-OR1528

2-(4-Chloro-phenyl)-4-hydroxy-thiazole-5-carboxylic acid ethyl ester

Ref: 10-F317442