CCCCCCCCCCCCCCCCOC1=CC=C(C=C1)C1=C(C(C)S(=O)(=O)C2=CC=C(NS(=O)(=O)C3=CC(N=NC4C(C)=NN(C4=O)C4=CC=CC=C4)=C(OC)C=C3)C=C2)C(=O)C=C(C)C1=O

InChIKey=ODKNTYSGNFUPOI-UHFFFAOYSA-N

C54H65N5O9S2

992.26

Organic compounds

Benzenoids

Benzene and substituted derivatives

Sulfanilides

Not available

Sulfanilides

Alpha amino acids and derivatives Benzenesulfonamides Benzenesulfonyl compounds Methoxyanilines Anisoles Phenoxy compounds Methoxybenzenes P-benzoquinones Alkyl aryl ethers Pyrazolones Organosulfonamides Sulfones Aminosulfonyl compounds Azo compounds Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds Hydrocarbon derivatives Organic oxides

Aromatic heteromonocyclic compounds

Sulfanilide - Alpha-amino acid or derivatives - Benzenesulfonamide - Methoxyaniline - Benzenesulfonyl group - Quinone - Phenol ether - Phenoxy compound - Methoxybenzene - P-benzoquinone - Anisole - Alkyl aryl ether - Pyrazolinone - Organosulfonic acid amide - Aminosulfonyl compound - Pyrazoline - Sulfone - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Azo compound - Ketone - Cyclic ketone - Organoheterocyclic compound - Azacycle - Ether - Carboxylic acid derivative - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Carbonyl group - Hydrocarbon derivative - Organic nitrogen compound - Organic oxide - 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