3-Chloro-N-(3-chloro-4-methoxyphenyl)propanamide is a chemical compound characterized by its amide functional group, which is derived from propanoic acid. The presence of two chlorine atoms and a methoxy group on the aromatic ring contributes to its unique reactivity and potential biological activity. The compound is likely to exhibit moderate to high lipophilicity due to the aromatic structure and the methoxy substituent, which can influence its solubility in organic solvents. The chlorinated phenyl group may enhance its interaction with biological targets, making it of interest in medicinal chemistry. Additionally, the amide bond can participate in hydrogen bonding, affecting its physical properties such as melting point and boiling point. This compound may be synthesized through specific organic reactions involving chlorination and amide formation, and its stability can be influenced by environmental factors such as pH and temperature. Overall, 3-chloro-N-(3-chloro-4-methoxyphenyl)propanamide represents a class of compounds that may have applications in pharmaceuticals or agrochemicals, pending further investigation into its biological properties.

3-chloro-N-(3-chloro-4-methoxyphenyl)propanamide

449170-55-2: 3-Chloro-N-(3-chloro-4-methoxyphenyl)propanamide is a chemical compound characterized by its amide functional group, which is derived from propanoic acid. The presence of two chlorine atoms and a methoxy group on the aromatic ring contributes to its unique reactivity and potential biological activity. The compound is likely to exhibit moderate to high lipophilicity due to the aromatic structure and the methoxy substituent, which can influence its solubility in organic solvents. The chlorinated phenyl group may enhance its interaction with biological targets, making it of interest in medicinal chemistry. Additionally, the amide bond can participate in hydrogen bonding, affecting its physical properties such as melting point and boiling point. This compound may be synthesized through specific organic reactions involving chlorination and amide formation, and its stability can be influenced by environmental factors such as pH and temperature. Overall, 3-chloro-N-(3-chloro-4-methoxyphenyl)propanamide represents a class of compounds that may have applications in pharmaceuticals or agrochemicals, pending further investigation into its biological properties.

CAS 449170-55-2

3-chloro-N-(3-chloro-4-methoxyphenyl)propanamide

3-Chloro-N-(3-chloro-4-methoxyphenyl)propanamide

Ref: 3D-ZSA17055