CCOC(=O)NC(=S)S[Sb](SC(=S)NC(=O)OCC)SC1=NC2=C(S1)C=C(C=C2)N=NC1=CC=C(NS(=O)(=O)C2=CC=C(NC(=O)C(SC3N=C=NC4=C3NC=N4)SC3=NC=NC4=C3NC=N4)C=C2)C=C1

InChIKey=BCJFETSJLHLXBL-UHFFFAOYSA-K

C39H32N15O7S9Sb

1233.08

Organic compounds

Benzenoids

Benzene and substituted derivatives

Sulfanilides

Not available

Sulfanilides

6-thiopurines Benzenesulfonamides Anilides Benzenesulfonyl compounds Benzothiazoles N-arylamides Alkylarylthioethers Pyrimidines and pyrimidine derivatives Organosulfonamides Thiazoles Aminosulfonyl compounds Carbamate esters Dithioacetals Heteroaromatic compounds Imidazoles Organic antimony salts Secondary carboxylic acid amides Azo compounds Carbodiimides Sulfenyl compounds Propargyl-type 1,3-dipolar organic compounds Dialkylthioethers Azacyclic compounds Organic oxides Carbonyl compounds Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Benzenesulfonamide - Sulfanilide - 6-thiopurine - 1,3-benzothiazole - Imidazopyrimidine - Benzenesulfonyl group - Purine - Anilide - Aryl thioether - N-arylamide - Alkylarylthioether - Pyrimidine - Organosulfonic acid amide - Azole - Thioacetal - Imidazole - Heteroaromatic compound - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Thiazole - Carbamic acid ester - Aminosulfonyl compound - Carboxamide group - Azo compound - Organic antimony salt - Secondary carboxylic acid amide - Organoheterocyclic compound - Dialkylthioether - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Organic metalloid salt - Organic metal salt - Sulfenyl compound - Carboxylic acid derivative - Thioether - Azacycle - Carbodiimide - Organic oxide - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Hydrocarbon derivative - Organic nitrogen compound - Carbonyl group - Organic oxygen compound - 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