Ethyl 4-acetyl-2-amino-5-methylfuran-3-carboxylate, with the CAS number 99076-38-7, is an organic compound characterized by its furan ring structure, which is a five-membered aromatic ring containing oxygen. This compound features an ethyl ester functional group, an acetyl group, and an amino group, contributing to its reactivity and potential biological activity. The presence of the amino group suggests that it may participate in various chemical reactions, such as nucleophilic substitutions or coupling reactions. The furan ring can also engage in electrophilic aromatic substitution due to its electron-rich nature. This compound may exhibit solubility in organic solvents, and its properties can be influenced by the presence of substituents on the furan ring. Ethyl 4-acetyl-2-amino-5-methylfuran-3-carboxylate may have applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to the structural motifs that are often associated with bioactive compounds. However, specific physical and chemical properties such as melting point, boiling point, and spectral data would require empirical measurement or literature reference for precise characterization.

ethyl 4-acetyl-2-amino-5-methylfuran-3-carboxylate

99076-38-7: Ethyl 4-acetyl-2-amino-5-methylfuran-3-carboxylate, with the CAS number 99076-38-7, is an organic compound characterized by its furan ring structure, which is a five-membered aromatic ring containing oxygen. This compound features an ethyl ester functional group, an acetyl group, and an amino group, contributing to its reactivity and potential biological activity. The presence of the amino group suggests that it may participate in various chemical reactions, such as nucleophilic substitutions or coupling reactions. The furan ring can also engage in electrophilic aromatic substitution due to its electron-rich nature. This compound may exhibit solubility in organic solvents, and its properties can be influenced by the presence of substituents on the furan ring. Ethyl 4-acetyl-2-amino-5-methylfuran-3-carboxylate may have applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to the structural motifs that are often associated with bioactive compounds. However, specific physical and chemical properties such as melting point, boiling point, and spectral data would require empirical measurement or literature reference for precise characterization.

CAS 99076-38-7

ethyl 4-acetyl-2-amino-5-methylfuran-3-carboxylate