3-(4-Methoxy-phenylamino)-propionic acid, identified by its CAS number 178425-91-7, is an organic compound characterized by the presence of a propionic acid backbone substituted with a 4-methoxyphenylamino group. This compound typically exhibits properties associated with both amino acids and aromatic compounds, including potential solubility in polar solvents due to the carboxylic acid functional group and the presence of the methoxy group, which can influence its reactivity and interaction with biological systems. The methoxy group may enhance lipophilicity, while the amino group can participate in hydrogen bonding, affecting the compound's overall stability and reactivity. Additionally, this compound may exhibit biological activity, making it of interest in pharmaceutical research, particularly in the development of drugs targeting specific pathways or conditions. Its structural features suggest potential applications in medicinal chemistry, where modifications to the aromatic ring or the propionic acid moiety could lead to derivatives with enhanced efficacy or selectivity.

3-(4-METHOXY-PHENYLAMINO)-PROPIONIC ACID

178425-91-7: 3-(4-Methoxy-phenylamino)-propionic acid, identified by its CAS number 178425-91-7, is an organic compound characterized by the presence of a propionic acid backbone substituted with a 4-methoxyphenylamino group. This compound typically exhibits properties associated with both amino acids and aromatic compounds, including potential solubility in polar solvents due to the carboxylic acid functional group and the presence of the methoxy group, which can influence its reactivity and interaction with biological systems. The methoxy group may enhance lipophilicity, while the amino group can participate in hydrogen bonding, affecting the compound's overall stability and reactivity. Additionally, this compound may exhibit biological activity, making it of interest in pharmaceutical research, particularly in the development of drugs targeting specific pathways or conditions. Its structural features suggest potential applications in medicinal chemistry, where modifications to the aromatic ring or the propionic acid moiety could lead to derivatives with enhanced efficacy or selectivity.

CAS 178425-91-7

3-(4-METHOXY-PHENYLAMINO)-PROPIONIC ACID

3-[(4-methoxyphenyl)amino]propanoic acid

Ref: IN-DA00261N

3-[(4-Methoxyphenyl)amino]propanoic acid

Ref: 3D-DHA42591