5-Amino-2-chlorobenzenesulfonamide, also known as sulfanilamide, is an organic compound characterized by the presence of an amino group (-NH2), a chlorobenzene ring, and a sulfonamide functional group (-SO2NH2). This compound is typically a white to off-white solid that is soluble in water and polar organic solvents. It exhibits properties typical of sulfonamides, including antibacterial activity, which is attributed to its ability to inhibit bacterial folic acid synthesis. The presence of the amino and sulfonamide groups contributes to its reactivity, allowing it to participate in various chemical reactions, such as acylation and alkylation. Additionally, the chlorine substituent on the benzene ring can influence the compound's biological activity and solubility. 5-Amino-2-chlorobenzenesulfonamide is used in pharmaceutical applications, particularly in the development of antimicrobial agents. Safety considerations include potential toxicity and the need for proper handling due to its chemical nature.

5-Amino-2-chlorobenzenesulfonamide

2015-19-2: 2-Chloro-5-aminobenzenesulfonamide, 3-Aminosulfonyl-4-chloroaniline, 3-Sulfamoyl-4-chloroaniline, 4-Chloro-3-sulfamoylaniline, 4-Chloro-5-(aminosulfonyl)aniline, Benzenesulfonamide, 5-Amino-2-Chloro-, Metanilamide, 6-chloro-, 5-Amino-2-chlorobenzenesulfonamide

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Applications 5-Amino-2-chlorobenzenesulfonamide (cas# 2015-19-2) is a compound useful in organic synthesis.
References Somers, F., et al.: Pharm. Pharmacol. Commun., 6, 89 (2000), D'Ambrosio, K., et al.: J. Med. Chem., 51, 3230 (2008),


CAS 2015-19-2: 5-Amino-2-chlorobenzenesulfonamide

5-Amino-2-chlorobenzenesulfonamide

Ref: 3D-FA17448

5-Amino-2-chlorobenzenesulfonamide

Ref: TR-A603425

5-Amino-2-chlorobenzenesulfonamide

Ref: 10-F545364

Benzenesulfonamide, 5-amino-2-chloro-

Ref: IN-DA002DGW