Ethyl 4-(chloromethyl)-2-(ethylamino)-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 an ethyl ester functional group, contributing to its solubility in organic solvents. The presence of a chloromethyl group indicates potential reactivity, making it useful in various synthetic applications. The ethylamino substituent enhances its biological activity, suggesting potential pharmacological properties. The thiazole moiety is often associated with diverse biological activities, including antimicrobial and anticancer effects. As a synthetic intermediate, this compound may be involved in the development of pharmaceuticals or agrochemicals. Its molecular structure and functional groups suggest it could participate in nucleophilic substitution reactions, particularly due to the electrophilic nature of the chloromethyl group. Overall, ethyl 4-(chloromethyl)-2-(ethylamino)-1,3-thiazole-5-carboxylate is a versatile compound with potential applications in medicinal chemistry and organic synthesis.

ethyl 4-(chloromethyl)-2-(ethylamino)-1,3-thiazole-5-carboxylate

937598-02-2: Ethyl 4-(chloromethyl)-2-(ethylamino)-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 an ethyl ester functional group, contributing to its solubility in organic solvents. The presence of a chloromethyl group indicates potential reactivity, making it useful in various synthetic applications. The ethylamino substituent enhances its biological activity, suggesting potential pharmacological properties. The thiazole moiety is often associated with diverse biological activities, including antimicrobial and anticancer effects. As a synthetic intermediate, this compound may be involved in the development of pharmaceuticals or agrochemicals. Its molecular structure and functional groups suggest it could participate in nucleophilic substitution reactions, particularly due to the electrophilic nature of the chloromethyl group. Overall, ethyl 4-(chloromethyl)-2-(ethylamino)-1,3-thiazole-5-carboxylate is a versatile compound with potential applications in medicinal chemistry and organic synthesis.

CAS 937598-02-2

ethyl 4-(chloromethyl)-2-(ethylamino)-1,3-thiazole-5-carboxylate