Ethyl 7-(4-dimethylaminophenyl)-7-oxo-heptanoate, identified by its CAS number 91727-04-7, is an organic compound characterized by its ester functional group and a ketone moiety. This compound features a heptanoate backbone, which consists of a seven-carbon chain, and is substituted at the 7-position with a 4-dimethylaminophenyl group, contributing to its unique chemical properties. The presence of the dimethylamino group enhances its electron-donating ability, potentially influencing its reactivity and solubility in various solvents. Ethyl esters like this compound are often used in organic synthesis and may exhibit biological activity, making them of interest in pharmaceutical research. The compound's structure suggests it may participate in various chemical reactions, including nucleophilic substitutions and condensation reactions. Its physical properties, such as boiling point, melting point, and solubility, would depend on the specific molecular interactions and the presence of functional groups. Overall, ethyl 7-(4-dimethylaminophenyl)-7-oxo-heptanoate represents a versatile structure in organic chemistry with potential applications in medicinal chemistry and material science.

ethyl 7-(4-dimethylaminophenyl)-7-oxo-heptanoate

91727-04-7: Ethyl 7-(4-dimethylaminophenyl)-7-oxo-heptanoate, identified by its CAS number 91727-04-7, is an organic compound characterized by its ester functional group and a ketone moiety. This compound features a heptanoate backbone, which consists of a seven-carbon chain, and is substituted at the 7-position with a 4-dimethylaminophenyl group, contributing to its unique chemical properties. The presence of the dimethylamino group enhances its electron-donating ability, potentially influencing its reactivity and solubility in various solvents. Ethyl esters like this compound are often used in organic synthesis and may exhibit biological activity, making them of interest in pharmaceutical research. The compound's structure suggests it may participate in various chemical reactions, including nucleophilic substitutions and condensation reactions. Its physical properties, such as boiling point, melting point, and solubility, would depend on the specific molecular interactions and the presence of functional groups. Overall, ethyl 7-(4-dimethylaminophenyl)-7-oxo-heptanoate represents a versatile structure in organic chemistry with potential applications in medicinal chemistry and material science.

CAS 91727-04-7

ethyl 7-(4-dimethylaminophenyl)-7-oxo-heptanoate

Ethyl 7-[4-(N,N-Dimethylamino)phenyl]-7-oxoheptanoate

Ref: 10-F208088