3-{(2-Methoxyphenyl)[(4-methylphenyl)sulfonyl]amino}propanoic acid, with the CAS number 103687-96-3, is an organic compound characterized by its complex structure, which includes a propanoic acid backbone, a sulfonamide functional group, and aromatic rings. This compound features a methoxy group on one aromatic ring and a methyl group on the para position of the other aromatic ring, contributing to its lipophilicity and potential biological activity. The sulfonyl group enhances the compound's solubility in polar solvents and may influence its reactivity and interaction with biological targets. As a derivative of amino acids, it may exhibit properties relevant to medicinal chemistry, including potential anti-inflammatory or analgesic effects. The presence of both hydrophilic (carboxylic acid) and hydrophobic (aromatic rings) components suggests that it could interact with various biological systems, making it a candidate for further pharmacological studies. However, specific biological activities and applications would require empirical investigation to elucidate its full potential.

3-{(2-METHOXYPHENYL)[(4-METHYLPHENYL)SULFONYL]AMINO}PROPANOIC ACID

103687-96-3: 3-{(2-Methoxyphenyl)[(4-methylphenyl)sulfonyl]amino}propanoic acid, with the CAS number 103687-96-3, is an organic compound characterized by its complex structure, which includes a propanoic acid backbone, a sulfonamide functional group, and aromatic rings. This compound features a methoxy group on one aromatic ring and a methyl group on the para position of the other aromatic ring, contributing to its lipophilicity and potential biological activity. The sulfonyl group enhances the compound's solubility in polar solvents and may influence its reactivity and interaction with biological targets. As a derivative of amino acids, it may exhibit properties relevant to medicinal chemistry, including potential anti-inflammatory or analgesic effects. The presence of both hydrophilic (carboxylic acid) and hydrophobic (aromatic rings) components suggests that it could interact with various biological systems, making it a candidate for further pharmacological studies. However, specific biological activities and applications would require empirical investigation to elucidate its full potential.

CAS 103687-96-3

3-{(2-METHOXYPHENYL)[(4-METHYLPHENYL)SULFONYL]AMINO}PROPANOIC ACID

3-[N-(2-Methoxyphenyl)4-methylbenzenesulfonamido]propanoic acid

Ref: 3D-DEA68796