Ethyl 2-amino-5-(4-chlorophenyl)thiazole-4-carboxylate, with the CAS number 77505-89-6, is a chemical compound characterized by its thiazole ring, which is a five-membered heterocyclic structure containing sulfur and nitrogen. This compound features an ethyl ester functional group, contributing to its solubility and reactivity. The presence of a 4-chlorophenyl group indicates that it has a chlorine substituent on a phenyl ring, which can influence its biological activity and lipophilicity. The amino group attached to the thiazole enhances its potential for hydrogen bonding and reactivity in various chemical reactions. Ethyl 2-amino-5-(4-chlorophenyl)thiazole-4-carboxylate may exhibit pharmacological properties, making it of interest in medicinal chemistry, particularly in the development of therapeutic agents. Its structural features suggest potential applications in drug design, where modifications to the thiazole or phenyl groups could lead to compounds with enhanced efficacy or selectivity. As with many organic compounds, its stability, reactivity, and biological activity would depend on the specific conditions under which it is used.

ethyl2-amino-5-(4-chlorophenyl)thiazole-4-carboxylate

77505-89-6: Ethyl 2-amino-5-(4-chlorophenyl)thiazole-4-carboxylate, with the CAS number 77505-89-6, is a chemical compound characterized by its thiazole ring, which is a five-membered heterocyclic structure containing sulfur and nitrogen. This compound features an ethyl ester functional group, contributing to its solubility and reactivity. The presence of a 4-chlorophenyl group indicates that it has a chlorine substituent on a phenyl ring, which can influence its biological activity and lipophilicity. The amino group attached to the thiazole enhances its potential for hydrogen bonding and reactivity in various chemical reactions. Ethyl 2-amino-5-(4-chlorophenyl)thiazole-4-carboxylate may exhibit pharmacological properties, making it of interest in medicinal chemistry, particularly in the development of therapeutic agents. Its structural features suggest potential applications in drug design, where modifications to the thiazole or phenyl groups could lead to compounds with enhanced efficacy or selectivity. As with many organic compounds, its stability, reactivity, and biological activity would depend on the specific conditions under which it is used.

CAS 77505-89-6

ethyl2-amino-5-(4-chlorophenyl)thiazole-4-carboxylate