CCN(C1=CC=CC=C1)S(=O)(=O)C1=CC(NC(=O)C2CCN(CC2)C2=NC=CN=C2)=C(OC)C=C1

InChIKey=LFXSHZRIMJLHOJ-UHFFFAOYSA-N

C25H29N5O4S

495.6

Organic compounds

Benzenoids

Benzene and substituted derivatives

Sulfanilides

Not available

Sulfanilides

Benzenesulfonamides Anilides Piperidinecarboxamides Benzenesulfonyl compounds Methoxyanilines Anisoles Phenoxy compounds Dialkylarylamines Methoxybenzenes N-arylamides Aminopyrazines Alkyl aryl ethers Organosulfonamides Imidolactams Heteroaromatic compounds Aminosulfonyl compounds Amino acids and derivatives Secondary carboxylic acid amides Azacyclic compounds Carbonyl compounds Hydrocarbon derivatives Organic oxides

Aromatic heteromonocyclic compounds

Sulfanilide - Benzenesulfonamide - Anilide - Methoxyaniline - Piperidinecarboxamide - Benzenesulfonyl group - N-arylamide - Dialkylarylamine - Phenoxy compound - Methoxybenzene - Anisole - Phenol ether - Alkyl aryl ether - Aminopyrazine - Pyrazine - Organosulfonic acid amide - Imidolactam - Piperidine - Heteroaromatic compound - Aminosulfonyl compound - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Amino acid or derivatives - Tertiary amine - Secondary carboxylic acid amide - Carboxamide group - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Ether - Amine - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - Organic oxygen compound - Organic oxide - Organonitrogen compound - Organooxygen compound - Organosulfur 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