Ethyl 5-amino-4-(4-bromophenyl)isoxazole-3-carboxylate, with the CAS number 925007-20-1, is a chemical compound characterized by its isoxazole ring structure, which is a five-membered heterocyclic compound containing both nitrogen and oxygen. This substance features an ethyl ester functional group, contributing to its solubility and reactivity. The presence of a bromophenyl group enhances its potential for biological activity, as halogenated aromatic compounds often exhibit unique pharmacological properties. The amino group at the 5-position of the isoxazole ring may participate in hydrogen bonding, influencing the compound's interactions in biological systems. Ethyl 5-amino-4-(4-bromophenyl)isoxazole-3-carboxylate is of interest in medicinal chemistry, particularly for its potential applications in drug development, as compounds with isoxazole moieties are often explored for their anti-inflammatory, antimicrobial, and anticancer activities. Its synthesis and characterization involve standard organic chemistry techniques, and it is typically handled with caution due to the presence of bromine, which can pose environmental and health risks.

ETHYL 5-AMINO-4-(4-BROMOPHENYL)ISOXAZOLE-3-CARBOXYLATE

925007-20-1: Ethyl 5-amino-4-(4-bromophenyl)isoxazole-3-carboxylate, with the CAS number 925007-20-1, is a chemical compound characterized by its isoxazole ring structure, which is a five-membered heterocyclic compound containing both nitrogen and oxygen. This substance features an ethyl ester functional group, contributing to its solubility and reactivity. The presence of a bromophenyl group enhances its potential for biological activity, as halogenated aromatic compounds often exhibit unique pharmacological properties. The amino group at the 5-position of the isoxazole ring may participate in hydrogen bonding, influencing the compound's interactions in biological systems. Ethyl 5-amino-4-(4-bromophenyl)isoxazole-3-carboxylate is of interest in medicinal chemistry, particularly for its potential applications in drug development, as compounds with isoxazole moieties are often explored for their anti-inflammatory, antimicrobial, and anticancer activities. Its synthesis and characterization involve standard organic chemistry techniques, and it is typically handled with caution due to the presence of bromine, which can pose environmental and health risks.

CAS 925007-20-1

ETHYL 5-AMINO-4-(4-BROMOPHENYL)ISOXAZOLE-3-CARBOXYLATE