3-Chloro-N-(2-chlorobenzyl)propanamide is a chemical compound characterized by its amide functional group, which is formed from the reaction of a carboxylic acid and an amine. This compound features a propanamide backbone with a chlorinated benzyl substituent, contributing to its unique properties. The presence of chlorine atoms in both the propanamide and the benzyl groups enhances its reactivity and may influence its biological activity. Typically, compounds like this may exhibit moderate to high lipophilicity due to the aromatic ring, which can affect their solubility in organic solvents and their interaction with biological membranes. The molecular structure suggests potential applications in pharmaceuticals or agrochemicals, where chlorinated compounds are often explored for their efficacy and specificity. Additionally, the compound's stability and reactivity can be influenced by the electronic effects of the chlorine substituents, making it a subject of interest in synthetic organic chemistry. Safety and handling precautions should be observed due to the presence of halogenated compounds, which may pose environmental and health risks.

3-CHLORO-N-(2-CHLOROBENZYL)PROPANAMIDE

103038-66-0: 3-Chloro-N-(2-chlorobenzyl)propanamide is a chemical compound characterized by its amide functional group, which is formed from the reaction of a carboxylic acid and an amine. This compound features a propanamide backbone with a chlorinated benzyl substituent, contributing to its unique properties. The presence of chlorine atoms in both the propanamide and the benzyl groups enhances its reactivity and may influence its biological activity. Typically, compounds like this may exhibit moderate to high lipophilicity due to the aromatic ring, which can affect their solubility in organic solvents and their interaction with biological membranes. The molecular structure suggests potential applications in pharmaceuticals or agrochemicals, where chlorinated compounds are often explored for their efficacy and specificity. Additionally, the compound's stability and reactivity can be influenced by the electronic effects of the chlorine substituents, making it a subject of interest in synthetic organic chemistry. Safety and handling precautions should be observed due to the presence of halogenated compounds, which may pose environmental and health risks.

CAS 103038-66-0

3-CHLORO-N-(2-CHLOROBENZYL)PROPANAMIDE

3-Chloro-N-(2-chlorobenzyl)propanamide

Ref: 3D-DEA03866