COC1=CC=CC=C1NS(=O)(=O)C1=C(NN=C(C)C2=CC3=C(OCCO3)C=C2)C=CC(=C1)[N+]([O-])=O

InChIKey=ZCKJCSJESTZJAG-UHFFFAOYSA-N

C23H22N4O7S

498.51

Organic compounds

Benzenoids

Benzene and substituted derivatives

Sulfanilides

Not available

Sulfanilides

Benzenesulfonamides Benzo-1,4-dioxanes Benzenesulfonyl compounds Methoxyanilines Nitrobenzenes Phenoxy compounds Phenylhydrazines Methoxybenzenes Nitroaromatic compounds Anisoles Alkyl aryl ethers Organosulfonamides Para dioxins Aminosulfonyl compounds Organic oxoazanium compounds Hydrazones Propargyl-type 1,3-dipolar organic compounds Oxacyclic compounds Organic salts Organic zwitterions Hydrocarbon derivatives Organopnictogen compounds Organic oxides

Aromatic heteropolycyclic compounds

Benzenesulfonamide - Benzo-1,4-dioxane - Benzodioxane - Sulfanilide - Benzenesulfonyl group - Nitrobenzene - Methoxyaniline - Phenoxy compound - Nitroaromatic compound - Anisole - Phenol ether - Methoxybenzene - Phenylhydrazine - Alkyl aryl ether - Para-dioxin - Organosulfonic acid amide - Aminosulfonyl compound - Sulfonyl - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - C-nitro compound - Organic nitro compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Ether - Hydrazone - Allyl-type 1,3-dipolar organic compound - Oxacycle - Organic oxoazanium - Organoheterocyclic compound - Hydrocarbon derivative - Organic oxide - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Organic nitrogen compound - Organic zwitterion - Organopnictogen compound - Organic salt - 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