Ethyl 4-(chloromethyl)-2-[(2-methoxyethyl)amino]-1,3-thiazole-5-carboxylate is a synthetic organic 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, contributing to its potential reactivity and solubility properties. The presence of a chloromethyl group indicates that it may participate in nucleophilic substitution reactions, making it a versatile intermediate in organic synthesis. Additionally, the methoxyethylamino substituent suggests potential biological activity, as amines can interact with various biological targets. The compound's molecular structure implies it may exhibit polar characteristics due to the presence of the carboxylate and ether functionalities, influencing its solubility in polar solvents. Overall, this compound may be of interest in medicinal chemistry and drug development, particularly in the design of thiazole-based pharmaceuticals. However, specific biological activity and safety profiles would require further investigation through empirical studies.

ethyl 4-(chloromethyl)-2-[(2-methoxyethyl)amino]-1,3-thiazole-5-carboxylate

937598-20-4: Ethyl 4-(chloromethyl)-2-[(2-methoxyethyl)amino]-1,3-thiazole-5-carboxylate is a synthetic organic 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, contributing to its potential reactivity and solubility properties. The presence of a chloromethyl group indicates that it may participate in nucleophilic substitution reactions, making it a versatile intermediate in organic synthesis. Additionally, the methoxyethylamino substituent suggests potential biological activity, as amines can interact with various biological targets. The compound's molecular structure implies it may exhibit polar characteristics due to the presence of the carboxylate and ether functionalities, influencing its solubility in polar solvents. Overall, this compound may be of interest in medicinal chemistry and drug development, particularly in the design of thiazole-based pharmaceuticals. However, specific biological activity and safety profiles would require further investigation through empirical studies.

CAS 937598-20-4

ethyl 4-(chloromethyl)-2-[(2-methoxyethyl)amino]-1,3-thiazole-5-carboxylate