3-Chloro-N-[4-(dimethylamino)phenyl]propanamide, identified by its CAS number 544667-97-2, is a chemical compound that features a propanamide backbone substituted with a chloro group and a dimethylamino phenyl moiety. This compound typically exhibits characteristics common to amides, such as moderate polarity due to the presence of the carbonyl group, which can engage in hydrogen bonding. The chloro substituent may influence its reactivity and solubility, potentially enhancing its lipophilicity. The dimethylamino group is known for its basicity and can participate in various chemical interactions, making the compound of interest in medicinal chemistry and drug design. Its structural features suggest potential applications in pharmaceuticals, particularly in the development of compounds with specific biological activities. The presence of both electron-donating and electron-withdrawing groups in its structure may also affect its electronic properties, influencing its behavior in chemical reactions and interactions with biological targets. Overall, this compound's unique structure positions it as a candidate for further investigation in various chemical and biological contexts.

3-chloro-N-[4-(dimethylamino)phenyl]propanamide

544667-97-2: 3-Chloro-N-[4-(dimethylamino)phenyl]propanamide, identified by its CAS number 544667-97-2, is a chemical compound that features a propanamide backbone substituted with a chloro group and a dimethylamino phenyl moiety. This compound typically exhibits characteristics common to amides, such as moderate polarity due to the presence of the carbonyl group, which can engage in hydrogen bonding. The chloro substituent may influence its reactivity and solubility, potentially enhancing its lipophilicity. The dimethylamino group is known for its basicity and can participate in various chemical interactions, making the compound of interest in medicinal chemistry and drug design. Its structural features suggest potential applications in pharmaceuticals, particularly in the development of compounds with specific biological activities. The presence of both electron-donating and electron-withdrawing groups in its structure may also affect its electronic properties, influencing its behavior in chemical reactions and interactions with biological targets. Overall, this compound's unique structure positions it as a candidate for further investigation in various chemical and biological contexts.

CAS 544667-97-2

3-chloro-N-[4-(dimethylamino)phenyl]propanamide

3-chloro-N-[4-(dimethylamino)phenyl]propanamide

Ref: IN-DA00DAT9

3-chloro-N-[4-(dimethylamino)phenyl]propanamide

Ref: 10-F315390