Cl.Cl.NC(=N)C1=CC=CC(\C=C\CN(C2=CC=C(OC3CCN(CC3)C3=NCCO3)C=C2)S(=O)(=O)CC(O)=O)=C1

InChIKey=SVSJYUVQBUVENK-IKXJGISXSA-N

C26H33Cl2N5O6S

614.54

Organic compounds

Benzenoids

Benzene and substituted derivatives

Sulfanilides

Not available

Sulfanilides

Piperidinecarboxamides Styrenes Phenoxy compounds Phenol ethers Alkyl aryl ethers Organosulfonamides Organic sulfonamides Oxazolines Aminosulfonyl compounds Isoureas Propargyl-type 1,3-dipolar organic compounds Oxacyclic compounds Azacyclic compounds Carboxamidines Carboximidamides Monocarboxylic acids and derivatives Carboxylic acids Amines Hydrocarbon derivatives Hydrochlorides Organic oxides Carbonyl compounds

Aromatic heteromonocyclic compounds

Sulfanilide - 1-piperidinecarboxamide - Piperidinecarboxamide - Phenoxy compound - Phenol ether - Styrene - Alkyl aryl ether - Piperidine - Organic sulfonic acid amide - Organosulfonic acid amide - Oxazoline - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Aminosulfonyl compound - Sulfonyl - Isourea - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Organoheterocyclic compound - Carboximidamide - Azacycle - Oxacycle - Amidine - Carboxylic acid amidine - Carboxylic acid derivative - Carboxylic acid - Ether - Monocarboxylic acid or derivatives - Hydrochloride - Organonitrogen compound - Organic nitrogen compound - Organooxygen compound - Organosulfur compound - Organic oxygen compound - Organic oxide - Carbonyl group - 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