3-Amino-N-(5-chloro-2-methoxyphenyl)benzamide is an organic compound characterized by its amine and amide functional groups, which contribute to its reactivity and potential biological activity. The presence of a chloro substituent on the aromatic ring enhances its lipophilicity, potentially influencing its interaction with biological targets. The methoxy group serves as an electron-donating substituent, which can affect the compound's electronic properties and steric hindrance. This compound may exhibit properties typical of aromatic amines, such as being a weak base due to the amino group, and it may participate in hydrogen bonding due to the amide functionality. Its structural features suggest potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, where modifications to the aromatic system can lead to variations in biological activity. Additionally, the compound's solubility and stability in various solvents can be influenced by its functional groups, making it a candidate for further study in drug formulation and design.

3-amino-N-(5-chloro-2-methoxyphenyl)benzamide

897594-66-0: 3-Amino-N-(5-chloro-2-methoxyphenyl)benzamide is an organic compound characterized by its amine and amide functional groups, which contribute to its reactivity and potential biological activity. The presence of a chloro substituent on the aromatic ring enhances its lipophilicity, potentially influencing its interaction with biological targets. The methoxy group serves as an electron-donating substituent, which can affect the compound's electronic properties and steric hindrance. This compound may exhibit properties typical of aromatic amines, such as being a weak base due to the amino group, and it may participate in hydrogen bonding due to the amide functionality. Its structural features suggest potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, where modifications to the aromatic system can lead to variations in biological activity. Additionally, the compound's solubility and stability in various solvents can be influenced by its functional groups, making it a candidate for further study in drug formulation and design.

CAS 897594-66-0

3-amino-N-(5-chloro-2-methoxyphenyl)benzamide