CN(C1=C(C)C=C(Br)C=C1C(=O)NO)S(=O)(=O)C1=CC=C(OCC#CCOC2CCCCO2)C=C1

InChIKey=VAHBOAURZYOQMQ-UHFFFAOYSA-N

C24H27BrN2O7S

567.45

Organic compounds

Benzenoids

Benzene and substituted derivatives

Sulfanilides

Not available

Sulfanilides

3-halobenzoic acids and derivatives Benzenesulfonamides m-Toluamides Benzenesulfonyl compounds Phenoxy compounds Phenol ethers Benzoyl derivatives Alkyl aryl ethers Bromobenzenes Oxanes Organosulfonamides Aryl bromides Vinylogous amides Aminosulfonyl compounds Hydroxamic acids Oxacyclic compounds Acetals Organobromides Organonitrogen compounds Organopnictogen compounds Organic oxides Hydrocarbon derivatives

Aromatic heteromonocyclic compounds

Sulfanilide - 3-halobenzoic acid or derivatives - Halobenzoic acid or derivatives - Benzenesulfonamide - Benzoic acid or derivatives - Toluamide - M-toluamide - Benzenesulfonyl group - Benzoyl - Phenoxy compound - Phenol ether - Alkyl aryl ether - Bromobenzene - Halobenzene - Toluene - Oxane - Aryl bromide - Organosulfonic acid amide - Aryl halide - Vinylogous amide - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Aminosulfonyl compound - Hydroxamic acid - Acetal - Oxacycle - Organoheterocyclic compound - Carboxylic acid derivative - Ether - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organosulfur compound - Organooxygen compound - Organohalogen compound - Organobromide - Organonitrogen 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