CCCC(=O)C1=CC(Cl)=C(N=C1CN1CCCC1=O)N1CCC(CC1)C(=O)N(C)S(=O)(=O)N(C)C1=CC=C(F)C=C1

InChIKey=GTJGWWOBVMWYGS-UHFFFAOYSA-N

C28H35ClFN5O5S

608.13

Organic compounds

Benzenoids

Benzene and substituted derivatives

Sulfanilides

Not available

Sulfanilides

Piperidinecarboxamides Aryl alkyl ketones Dialkylarylamines Aminopyridines and derivatives Fluorobenzenes Pyrrolidine-2-ones Aryl chlorides Aryl fluorides N-alkylpyrrolidines Imidolactams Tertiary carboxylic acid amides Organic sulfuric acids and derivatives Heteroaromatic compounds Lactams Azacyclic compounds Organic oxides Organofluorides Organochlorides Hydrocarbon derivatives

Aromatic heteromonocyclic compounds

Sulfanilide - Piperidinecarboxamide - Aryl ketone - Aryl alkyl ketone - Dialkylarylamine - Halobenzene - Fluorobenzene - Aminopyridine - Aryl halide - Piperidine - Pyridine - Pyrrolidone - 2-pyrrolidone - Aryl fluoride - N-alkylpyrrolidine - Aryl chloride - Imidolactam - Organic sulfuric acid or derivatives - Pyrrolidine - Heteroaromatic compound - Tertiary carboxylic acid amide - Carboxamide group - Lactam - Ketone - Azacycle - Carboxylic acid derivative - Organoheterocyclic compound - Organic oxide - Organohalogen compound - Organochloride - Organofluoride - Organonitrogen compound - Organooxygen compound - Carbonyl group - Organic nitrogen compound - Organic oxygen compound - Amine - Hydrocarbon derivative - 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