CC(C)(C)C1=CC(=C(OCCOCCOC2=C(C=C(C=C2)C(C)(C)C)S(=O)(=O)NC2=CC=C(C=C2)[N+]([O-])=O)C=C1)S(=O)(=O)NC1=CC=C(C=C1)[N+]([O-])=O

InChIKey=OKJVJMASCLRMSJ-UHFFFAOYSA-N

C36H42N4O11S2

770.87

Organic compounds

Benzenoids

Benzene and substituted derivatives

Sulfanilides

Not available

Sulfanilides

Benzenesulfonamides Phenylpropanes Benzenesulfonyl compounds Nitrobenzenes Phenoxy compounds Phenol ethers Nitroaromatic compounds Alkyl aryl ethers Organosulfonamides Aminosulfonyl compounds Propargyl-type 1,3-dipolar organic compounds Dialkyl ethers Organic oxoazanium compounds Organopnictogen compounds Organic zwitterions Hydrocarbon derivatives Organonitrogen compounds Organic oxides

Aromatic homomonocyclic compounds

Benzenesulfonamide - Sulfanilide - Phenylpropane - Benzenesulfonyl group - Nitrobenzene - Phenoxy compound - Nitroaromatic compound - Phenol ether - Alkyl aryl ether - Organosulfonic acid amide - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Aminosulfonyl compound - Sulfonyl - C-nitro compound - Organic nitro compound - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Ether - Dialkyl ether - Organic oxoazanium - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Organosulfur compound - Organic zwitterion - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Aromatic homomonocyclic 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