CC1=NN(C(=O)C1N=NC1=CC(=C(C)C=C1)S(=O)(=O)NC1=CC=CC=C1)C1=CC(Cl)=C(C=C1Cl)S(O)(=O)=O

InChIKey=QWPUVKFRCUDYSR-UHFFFAOYSA-N

C23H19Cl2N5O6S2

596.45

Organic compounds

Benzenoids

Benzene and substituted derivatives

Sulfanilides

Not available

Sulfanilides

Alpha amino acids and derivatives Benzenesulfonic acids and derivatives Benzenesulfonamides 1-sulfo,2-unsubstituted aromatic compounds Benzenesulfonyl compounds Dichlorobenzenes Toluenes Pyrazolones Organosulfonamides Aryl chlorides Organosulfonic acids Aminosulfonyl compounds Azo compounds Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds Carbonyl compounds Hydrocarbon derivatives Organic oxides Organochlorides

Aromatic heteromonocyclic compounds

Alpha-amino acid or derivatives - Benzenesulfonamide - Sulfanilide - Benzenesulfonate - Arylsulfonic acid or derivatives - Benzenesulfonyl group - 1-sulfo,2-unsubstituted aromatic compound - 1,4-dichlorobenzene - Chlorobenzene - Halobenzene - Toluene - Aryl chloride - Organosulfonic acid amide - Pyrazolinone - Aryl halide - Sulfonyl - Organosulfonic acid - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Pyrazoline - Aminosulfonyl compound - Azo compound - Organoheterocyclic compound - Azacycle - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Carboxylic acid derivative - Organosulfur compound - Hydrocarbon derivative - Organic nitrogen compound - Carbonyl group - Organic oxide - Organohalogen compound - Organic oxygen compound - Organochloride - Organonitrogen compound - Organooxygen compound - Aromatic heteromonocyclic 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