Methyl 2-amino-5-phenyl-1,3-thiazole-4-carboxylate, with the CAS number 115174-39-5, is a chemical compound characterized by its thiazole ring structure, which incorporates both sulfur and nitrogen atoms. This compound features an amino group and a carboxylate ester, contributing to its potential reactivity and solubility in various solvents. The presence of a phenyl group enhances its aromatic characteristics, which may influence its biological activity and interactions. Typically, compounds of this nature are studied for their potential applications in pharmaceuticals, agrochemicals, or as intermediates in organic synthesis. The thiazole moiety is often associated with various biological activities, making this compound of interest in medicinal chemistry. Its molecular structure suggests it may participate in hydrogen bonding and other intermolecular interactions, which can affect its physical properties such as melting point, boiling point, and solubility. Overall, methyl 2-amino-5-phenyl-1,3-thiazole-4-carboxylate is a versatile compound with potential applications in various fields of chemistry and biology.

METHYL 2-AMINO-5-PHENYL-1,3-THIAZOLE-4-CARBOXYLATE

115174-39-5: Methyl 2-amino-5-phenyl-1,3-thiazole-4-carboxylate, with the CAS number 115174-39-5, is a chemical compound characterized by its thiazole ring structure, which incorporates both sulfur and nitrogen atoms. This compound features an amino group and a carboxylate ester, contributing to its potential reactivity and solubility in various solvents. The presence of a phenyl group enhances its aromatic characteristics, which may influence its biological activity and interactions. Typically, compounds of this nature are studied for their potential applications in pharmaceuticals, agrochemicals, or as intermediates in organic synthesis. The thiazole moiety is often associated with various biological activities, making this compound of interest in medicinal chemistry. Its molecular structure suggests it may participate in hydrogen bonding and other intermolecular interactions, which can affect its physical properties such as melting point, boiling point, and solubility. Overall, methyl 2-amino-5-phenyl-1,3-thiazole-4-carboxylate is a versatile compound with potential applications in various fields of chemistry and biology.

CAS 115174-39-5

METHYL 2-AMINO-5-PHENYL-1,3-THIAZOLE-4-CARBOXYLATE

4-Thiazolecarboxylic acid, 2-amino-5-phenyl-, methyl ester, hydrochloride (1:1)

Ref: IN-DA000GDF