CCCC(=O)C1=C(CN2CCCC2=O)N=C(N2CCC(CC2)C(=O)NS(=O)(=O)NC2=CC=C(F)C=C2)C(=C1)C#N

InChIKey=WODCLRDVLZXKOG-UHFFFAOYSA-N

C27H31FN6O5S

570.64

Organic compounds

Benzenoids

Benzene and substituted derivatives

Sulfanilides

Not available

Sulfanilides

Piperidinecarboxamides 3-pyridinecarbonitriles Aryl alkyl ketones Dialkylarylamines Aminopyridines and derivatives Fluorobenzenes Pyrrolidine-2-ones N-alkylpyrrolidines Imidolactams Aryl fluorides Tertiary carboxylic acid amides Organic sulfuric acids and derivatives Heteroaromatic compounds Lactams Nitriles Azacyclic compounds Organofluorides Hydrocarbon derivatives Organic oxides

Aromatic heteromonocyclic compounds

Sulfanilide - Piperidinecarboxamide - Aryl ketone - Aryl alkyl ketone - 3-pyridinecarbonitrile - Dialkylarylamine - Aminopyridine - Fluorobenzene - Halobenzene - Aryl fluoride - Aryl halide - Piperidine - Pyridine - Pyrrolidone - 2-pyrrolidone - N-alkylpyrrolidine - Imidolactam - Pyrrolidine - Heteroaromatic compound - Tertiary carboxylic acid amide - Organic sulfuric acid or derivatives - Carboxamide group - Ketone - Lactam - Organoheterocyclic compound - Carboxylic acid derivative - Azacycle - Nitrile - Carbonitrile - Organic nitrogen compound - Organohalogen compound - Organofluoride - Cyanide - Organic oxygen compound - Carbonyl group - Hydrocarbon derivative - Organonitrogen compound - Organooxygen compound - Organic oxide - Amine - 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