4-Chlorobenzenesulfonamide

CAS : 98-64-6

Ref. 3D-FC20190

Informations sur le produit

• Nom: 4-Chlorobenzenesulfonamide
• Synonymes: 4-Chlorophenylsulfonamidep-Chlorobenzenesulfonamidep-Chlorophenylsulfonamide, 4-Chlorobenzenesulphonamide, 4-Chlorobenzezne sulfonamide, 4-Chlorophenylsulfonamide, Add 55051, Benzenesulfonamide, 4-chloro-, Benzenesulfonamide, p-chloro-, NSC 403674, NSC 9913, P-chlorobenzene sulfonamide, p-Chlorobenzenesulfamide, p-Chlorobenzenesulfonamide, p-Chlorophenylsulfonamide

Description

4-Chlorobenzenesulfonamide is a hydrogen bond acceptor and donor, which can form strong bonds with metal ions. It has been shown to have a high reaction yield in vitro. 4-Chlorobenzenesulfonamide has been shown to be active against human lymphocytes and rat hepatocytes in vitro. The drug is used as a pharmaceutical dosage for the treatment of tuberculosis. The hydrolysis process is initiated by acidification of the medium, which leads to the release of 4-chlorobenzenesulfonic acid from the salt. This process can be accelerated by adding hydrochloric acid or sodium hydroxide to the reaction mixture. 4-Chlorobenzenesulfonamide reacts with fluorine gas in an acidic environment to form an organic fluoride compound, which then reacts with water to form hydrofluoric acid and other products. Hydrofluoric acid is released from this reaction and diffuses into the surrounding tissue, where it

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 191.64 g/mol
• Formule: C₆H₆ClNO₂S
• Degré de pureté: Min. 95%
• InChI: InChI=1S/C6H6ClNO2S/c7-5-1-3-6(4-2-5)11(8,9)10/h1-4H,(H2,8,9,10)
• Code InChI: InChIKey=HHHDJHHNEURCNV-UHFFFAOYSA-N
• SMILES: NS(=O)(=O)c1ccc(Cl)cc1