Ethyl 2-(4-aminophenyl)-1,3-oxazole-4-carboxylate is a chemical compound characterized by its oxazole ring, which is a five-membered heterocyclic structure containing both nitrogen and oxygen. This compound features an ethyl ester functional group, contributing to its solubility and reactivity. The presence of the 4-aminophenyl group indicates that it has an amino substituent on a phenyl ring, which can participate in various chemical reactions, including electrophilic aromatic substitution and hydrogen bonding. The carboxylate moiety enhances its potential as a building block in organic synthesis and medicinal chemistry. This compound may exhibit biological activity due to its structural features, making it of interest in pharmaceutical research. Its molecular structure suggests potential applications in drug development, particularly in targeting specific biological pathways. Additionally, the compound's stability and reactivity can be influenced by factors such as pH and solvent conditions, which are important considerations in both laboratory and industrial settings.

ethyl 2-(4-aminophenyl)-1,3-oxazole-4-carboxylate

391248-21-8: Ethyl 2-(4-aminophenyl)-1,3-oxazole-4-carboxylate is a chemical compound characterized by its oxazole ring, which is a five-membered heterocyclic structure containing both nitrogen and oxygen. This compound features an ethyl ester functional group, contributing to its solubility and reactivity. The presence of the 4-aminophenyl group indicates that it has an amino substituent on a phenyl ring, which can participate in various chemical reactions, including electrophilic aromatic substitution and hydrogen bonding. The carboxylate moiety enhances its potential as a building block in organic synthesis and medicinal chemistry. This compound may exhibit biological activity due to its structural features, making it of interest in pharmaceutical research. Its molecular structure suggests potential applications in drug development, particularly in targeting specific biological pathways. Additionally, the compound's stability and reactivity can be influenced by factors such as pH and solvent conditions, which are important considerations in both laboratory and industrial settings.

CAS 391248-21-8

ethyl 2-(4-aminophenyl)-1,3-oxazole-4-carboxylate

Ethyl 2-(4'-aminophenyl)-1,3-oxazole-4-carboxylate

Ref: IN-DA00BYWX

Ethyl 2-(4′-aminophenyl)-1,3-oxazole-4-carboxylate

Ref: 10-F011712