3-Chloro-N-[4-(1-methylpropyl)phenyl]propanamide, identified by its CAS number 20331-29-7, is an organic compound characterized by its amide functional group, which is linked to a propanamide backbone. The presence of a chlorine atom at the third position of the propanamide chain contributes to its reactivity and potential biological activity. The compound features a phenyl group substituted with a 1-methylpropyl group, which enhances its hydrophobic characteristics and may influence its interaction with biological systems. This structural arrangement suggests potential applications in pharmaceuticals or agrochemicals, where such compounds often exhibit specific biological activities. The molecular structure indicates that it may participate in hydrogen bonding due to the amide group, affecting its solubility and stability in various solvents. Additionally, the presence of the chlorine atom may impart unique electronic properties, influencing its reactivity in chemical reactions. Overall, the characteristics of this compound make it a subject of interest in synthetic organic chemistry and medicinal chemistry research.

3-chloro-N-[4-(1-methylpropyl)phenyl]propanamide

20331-29-7: 3-Chloro-N-[4-(1-methylpropyl)phenyl]propanamide, identified by its CAS number 20331-29-7, is an organic compound characterized by its amide functional group, which is linked to a propanamide backbone. The presence of a chlorine atom at the third position of the propanamide chain contributes to its reactivity and potential biological activity. The compound features a phenyl group substituted with a 1-methylpropyl group, which enhances its hydrophobic characteristics and may influence its interaction with biological systems. This structural arrangement suggests potential applications in pharmaceuticals or agrochemicals, where such compounds often exhibit specific biological activities. The molecular structure indicates that it may participate in hydrogen bonding due to the amide group, affecting its solubility and stability in various solvents. Additionally, the presence of the chlorine atom may impart unique electronic properties, influencing its reactivity in chemical reactions. Overall, the characteristics of this compound make it a subject of interest in synthetic organic chemistry and medicinal chemistry research.

CAS 20331-29-7

3-chloro-N-[4-(1-methylpropyl)phenyl]propanamide

N-(4-sec-Butylphenyl)-3-chloropropanamide

Ref: IN-DA0028TK

N-(4-sec-butylphenyl)-3-chloropropanamide

Ref: 10-F314090