[Pd].[S-]C1=NC2=C(S1)C=C(C=C2)N=NC1=CC=C(NS(=O)(=O)C2=CC=C(NC(=O)C(N3CC3)(N3CC3)N3CC3)C=C2)C=C1

InChIKey=OBVFUKUOTXUUQM-UHFFFAOYSA-M

C27H25N8O3PdS3

712.15

Organic compounds

Benzenoids

Benzene and substituted derivatives

Sulfanilides

Not available

Sulfanilides

Alpha amino acids and derivatives Benzenesulfonamides Anilides Benzenesulfonyl compounds Benzothiazoles N-arylamides Organosulfonamides Thiazoles Aminosulfonyl compounds Heteroaromatic compounds Secondary carboxylic acid amides Orthocarboxylic acid derivatives Ortho amides Azo compounds Organic transition metal salts Azacyclic compounds Aziridines Organic oxides Carbonyl compounds Hydrocarbon derivatives Organic anions

Aromatic heteropolycyclic compounds

Alpha-amino acid or derivatives - Benzenesulfonamide - Sulfanilide - Benzenesulfonyl group - 1,3-benzothiazole - Anilide - N-arylamide - Organosulfonic acid amide - Azole - Heteroaromatic compound - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Aminosulfonyl compound - Thiazole - Sulfonyl - Azo compound - Carboxamide group - Ortho amide - Orthocarboxylic acid derivative - Secondary carboxylic acid amide - Aziridine - Carboxylic acid derivative - Azacycle - Organic transition metal salt - Organoheterocyclic compound - Organic nitrogen compound - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organic anion - 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