Ethyl 4-(2,3-dimethoxyphenyl)-4-oxo-butanoate, identified by its CAS number 898758-05-9, is an organic compound characterized by its ester functional group and a ketone moiety. This compound features a butanoate backbone, which is substituted at the fourth carbon with a 2,3-dimethoxyphenyl group, contributing to its aromatic properties. The presence of methoxy groups enhances its solubility in organic solvents and may influence its reactivity and biological activity. Typically, compounds of this nature are studied for their potential applications in pharmaceuticals, agrochemicals, or as intermediates in organic synthesis. The molecular structure suggests that it may exhibit interesting chemical behavior, such as undergoing nucleophilic attacks or participating in condensation reactions. Additionally, the compound's physical properties, such as melting point, boiling point, and solubility, would be influenced by its molecular weight and the presence of functional groups. Overall, ethyl 4-(2,3-dimethoxyphenyl)-4-oxo-butanoate represents a class of compounds with diverse applications in chemical research and industry.

ethyl 4-(2,3-dimethoxyphenyl)-4-oxo-butanoate

898758-05-9: Ethyl 4-(2,3-dimethoxyphenyl)-4-oxo-butanoate, identified by its CAS number 898758-05-9, is an organic compound characterized by its ester functional group and a ketone moiety. This compound features a butanoate backbone, which is substituted at the fourth carbon with a 2,3-dimethoxyphenyl group, contributing to its aromatic properties. The presence of methoxy groups enhances its solubility in organic solvents and may influence its reactivity and biological activity. Typically, compounds of this nature are studied for their potential applications in pharmaceuticals, agrochemicals, or as intermediates in organic synthesis. The molecular structure suggests that it may exhibit interesting chemical behavior, such as undergoing nucleophilic attacks or participating in condensation reactions. Additionally, the compound's physical properties, such as melting point, boiling point, and solubility, would be influenced by its molecular weight and the presence of functional groups. Overall, ethyl 4-(2,3-dimethoxyphenyl)-4-oxo-butanoate represents a class of compounds with diverse applications in chemical research and industry.

CAS 898758-05-9

ethyl 4-(2,3-dimethoxyphenyl)-4-oxo-butanoate