[Zn++].CCOC(=O)NC([SH2+])=[SH+].ClC(Cl)C(=O)NC1=CC=C(C=C1)S(=O)(=O)NC1=CC=C(C=C1)N=NC1=CC2=C([N-]C(=[SH+])[SH+]2)C=C1

InChIKey=UCSBGPGEGIYIKI-UHFFFAOYSA-Q

C25H25Cl2N6O5S5Zn

786.09

Organic compounds

Benzenoids

Benzene and substituted derivatives

Sulfanilides

Not available

Sulfanilides

Benzenesulfonamides Anilides Benzenesulfonyl compounds Benzothiazoles N-arylamides Organosulfonamides Thiazoles Aminosulfonyl compounds Carbamate esters Secondary carboxylic acid amides Azo compounds Organic transition metal salts Azacyclic compounds Organic metal halides Alkyl chlorides Organic oxides Organochlorides Hydrocarbon derivatives Carbonyl compounds Organic cations

Not available

Benzenesulfonamide - Sulfanilide - Benzo-thiazole - 1,2-benzothiazole - 1,3-benzothiazole - Benzenesulfonyl group - Anilide - N-arylamide - Organosulfonic acid amide - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Thiazole - Aminosulfonyl compound - Carbamic acid ester - Azo compound - Carboxamide group - Secondary carboxylic acid amide - Organic transition metal salt - Azacycle - Organoheterocyclic compound - Organic metal halide - Carboxylic acid derivative - Organic salt - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organochloride - Organohalogen compound - Organosulfur compound - Alkyl halide - Carbonyl group - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Alkyl chloride - Organic cation - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as sulfanilides. These are organic aromatic compounds containing a sulfanilide moiety, with the general structure RS(=O)(=O)NC1=CC=CC=C1.

Not available