Ethyl 7-(4-methoxy-3-nitro-phenyl)-7-oxo-heptanoate is an organic compound characterized by its ester functional group, which is derived from the reaction of a carboxylic acid and an alcohol. This compound features a heptanoate backbone, indicating a seven-carbon chain, with a ketone group at the seventh position and a substituted phenyl group that includes both a methoxy and a nitro group. The presence of the methoxy group suggests that the compound may exhibit certain electron-donating properties, while the nitro group is an electron-withdrawing group, which can influence the compound's reactivity and polarity. The overall structure indicates potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to the presence of functional groups that can participate in various chemical reactions. Additionally, the compound's molecular characteristics may affect its solubility, stability, and biological activity, making it a subject of interest for further research in organic synthesis and drug development.

ethyl 7-(4-methoxy-3-nitro-phenyl)-7-oxo-heptanoate

898758-95-7: Ethyl 7-(4-methoxy-3-nitro-phenyl)-7-oxo-heptanoate is an organic compound characterized by its ester functional group, which is derived from the reaction of a carboxylic acid and an alcohol. This compound features a heptanoate backbone, indicating a seven-carbon chain, with a ketone group at the seventh position and a substituted phenyl group that includes both a methoxy and a nitro group. The presence of the methoxy group suggests that the compound may exhibit certain electron-donating properties, while the nitro group is an electron-withdrawing group, which can influence the compound's reactivity and polarity. The overall structure indicates potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to the presence of functional groups that can participate in various chemical reactions. Additionally, the compound's molecular characteristics may affect its solubility, stability, and biological activity, making it a subject of interest for further research in organic synthesis and drug development.

CAS 898758-95-7

ethyl 7-(4-methoxy-3-nitro-phenyl)-7-oxo-heptanoate

Ethyl 7-(4-methoxy-3-nitrophenyl)-7-oxoheptanoate

Ref: 10-F208077