Methyl 4-methyl-2-phenyl-thiazole-5-carboxylate, identified by its CAS number 189271-66-7, is an organic compound characterized by its thiazole ring, which is a five-membered heterocyclic structure containing sulfur and nitrogen. This compound features a methyl group and a phenyl group, contributing to its aromatic properties and potentially influencing its reactivity and solubility. The carboxylate functional group indicates that it can participate in various chemical reactions, such as esterification or nucleophilic substitution. Typically, compounds like this may exhibit biological activity, making them of interest in pharmaceutical research. The presence of both the thiazole and phenyl groups suggests potential applications in medicinal chemistry, particularly in the development of new drugs or agrochemicals. Additionally, the methyl ester functionality may enhance lipophilicity, affecting the compound's absorption and distribution in biological systems. Overall, methyl 4-methyl-2-phenyl-thiazole-5-carboxylate is a versatile compound with potential applications in various fields, including organic synthesis and medicinal chemistry.

methyl 4-methyl-2-phenyl-thiazole-5-carboxylate

189271-66-7: Methyl 4-methyl-2-phenyl-thiazole-5-carboxylate, identified by its CAS number 189271-66-7, is an organic compound characterized by its thiazole ring, which is a five-membered heterocyclic structure containing sulfur and nitrogen. This compound features a methyl group and a phenyl group, contributing to its aromatic properties and potentially influencing its reactivity and solubility. The carboxylate functional group indicates that it can participate in various chemical reactions, such as esterification or nucleophilic substitution. Typically, compounds like this may exhibit biological activity, making them of interest in pharmaceutical research. The presence of both the thiazole and phenyl groups suggests potential applications in medicinal chemistry, particularly in the development of new drugs or agrochemicals. Additionally, the methyl ester functionality may enhance lipophilicity, affecting the compound's absorption and distribution in biological systems. Overall, methyl 4-methyl-2-phenyl-thiazole-5-carboxylate is a versatile compound with potential applications in various fields, including organic synthesis and medicinal chemistry.

CAS 189271-66-7

methyl 4-methyl-2-phenyl-thiazole-5-carboxylate

Methyl 4-methyl-2-phenylthiazole-5-carboxylate

Ref: IN-DA002I5J

Methyl 2-phenylthiazole-5-carboxylate

Ref: 54-OR300667