4-[(Phenylsulfonyl)amino]benzoic acid, also known by its CAS number 28547-16-2, is an organic compound characterized by the presence of both a benzoic acid moiety and a phenylsulfonyl group. This compound features an amino group attached to the para position of the benzoic acid, which enhances its solubility in polar solvents. The sulfonyl group contributes to its potential as a sulfonamide derivative, which may exhibit biological activity, including antimicrobial properties. The presence of the phenyl group can also influence the compound's electronic properties and steric hindrance. Typically, such compounds are studied for their applications in pharmaceuticals, particularly in drug design and development, due to their ability to interact with biological targets. The compound is likely to be a solid at room temperature, with moderate melting and boiling points, and may exhibit moderate to high stability under standard conditions. Its reactivity can be influenced by the functional groups present, making it a candidate for various chemical reactions, including coupling and substitution reactions.

4-[(phenylsulfonyl)amino]benzoic acid

28547-16-2: Benzoic acid, 4-[(phenylsulfonyl)amino]-

Benzoic acid, 4-[(phenylsulfonyl)amino]-

4-Benzenesulfonylaminobenzoic acid

4-[(Phenylsulfonyl)amino]benzoic acid is a chemical compound that is used as an organic reagent. It has cytotoxic effects on human cell lines and can induce apoptosis by binding to the sulfhydryl groups of cysteine residues in proteins. This compound also reacts with thiourea to form phenylhydrazone, which can react with benzene to form enaminones.

CAS 28547-16-2: 4-[(phenylsulfonyl)amino]benzoic acid

Benzoic acid, 4-[(phenylsulfonyl)amino]-

Ref: IN-DA002VO2

4-Benzenesulfonylaminobenzoic acid

Ref: 10-F015558

4-[(Phenylsulfonyl)amino]benzoic acid

Ref: 3D-FP136712