4-Amino-6-chloro-1,3-benzenedisulfonamide

CAS : 121-30-2

Ref. 3D-FA17655

Informations sur le produit

• Nom: 4-Amino-6-chloro-1,3-benzenedisulfonamide
• Synonymes: 4-Amino-6-chloro-m-benzenedisulfonamide3-Chloro-4,6-disulfamoylaniline5-Chloro-2,4-disulfamoylaniline, 1,3-Benzenedisulfonamide, 4-amino-6-chloro-, 1-Amino-5-chloro-2,4-benzenedisulfonamide, 3-Chloro-4,6-disulfamoylaniline, 4-Amino-6-Chloro-1,3-Benzene Disulfonamide, 4-Amino-6-Chloro-1,3-Benzenedisulphonamide, 4-Amino-6-Chloro-1,3-Benzenedisulphonamide (Dsa), 4-Amino-6-Chlorobenzen-1,3-Disulphonamide, 4-Amino-6-chloro-m-benzenedisulfonamide, 4-Amino-6-chlorobenzene-1,3-disulfonamide, 4-Amino-6-chlorobenzene-1,3-disulphonamide, 4-Ao-6-Chloro-1,3-Benzenedisulphonamide, 5-Chloro-2,4-disulfamoylaniline, Chloraminophenamide, Chloraophenamide, Chloroaminophenamide, Idorese, NSC 93772, Salamid, Salamide, Salamide (diuretic), Salmid, Su 5683, m-Benzenedisulfonamide, 4-amino-6-chloro-

Description

4-Amino-6-chloro-1,3-benzenedisulfonamide is a natural substance that has been used in Chinese medicine preparations for the treatment of cardiac problems. It belongs to the class of organic compounds called benzenedisulfonamides. 4-Amino-6-chloro-1,3-benzenedisulfonamide is produced by the bacterial enzyme aminase from amino acid and benzoic acid. The adsorption mechanism of 4-Amino-6-chloro-1,3-benzenedisulfonamide is not fully understood, but it is believed that the benzyl groups are key players in this process. The high affinity of 4-Amino-6-chloro1,3 benzenedisulfonamide to proteins may be due to its ability to form hydrogen bonds with protein side chains, such as serine or threonine residues. 4 Amino

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 285.73 g/mol
• Formule: C₆H₈ClN₃O₄S₂
• Degré de pureté: Min. 95%
• Couleur/Forme: White To Light Brown Solid
• InChI: InChI=1S/C6H8ClN3O4S2/c7-3-1-4(8)6(16(10,13)14)2-5(3)15(9,11)12/h1-2H,8H2,(H2,9,11,12)(H2,10,13,14)
• Code InChI: InChIKey=IHJCXVZDYSXXFT-UHFFFAOYSA-N
• SMILES: Nc1cc(Cl)c(S(N)(=O)=O)cc1S(N)(=O)=O