COC1=CC=C(NS(=O)(=O)C2=C(Cl)C=CC(NC(=O)C=CC3=CC=C(Br)O3)=C2)C=C1

InChIKey=YNEVVJJGDQOUHE-UHFFFAOYSA-N

C20H16BrClN2O5S

511.77

Organic compounds

Benzenoids

Benzene and substituted derivatives

Sulfanilides

Not available

Sulfanilides

Benzenesulfonamides Benzenesulfonyl compounds Methoxyanilines Anilides Phenoxy compounds Methoxybenzenes N-arylamides Anisoles Chlorobenzenes Alkyl aryl ethers Organosulfonamides Aryl bromides Aryl chlorides Heteroaromatic compounds Furans Aminosulfonyl compounds Secondary carboxylic acid amides Oxacyclic compounds Carbonyl compounds Hydrocarbon derivatives Organic oxides Organobromides Organochlorides Organopnictogen compounds

Aromatic heteromonocyclic compounds

Benzenesulfonamide - Sulfanilide - Benzenesulfonyl group - Anilide - Methoxyaniline - Anisole - Phenoxy compound - Phenol ether - N-arylamide - Methoxybenzene - Alkyl aryl ether - Chlorobenzene - Halobenzene - Organosulfonic acid amide - Aryl bromide - Aryl chloride - Aryl halide - Aminosulfonyl compound - Sulfonyl - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Heteroaromatic compound - Furan - Secondary carboxylic acid amide - Carboxamide group - Oxacycle - Organoheterocyclic compound - Carboxylic acid derivative - Ether - Hydrocarbon derivative - Organohalogen compound - Organic nitrogen compound - Organobromide - Organochloride - Carbonyl group - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Organopnictogen 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