Cl.Cl.CCOC(=O)CS(=O)(=O)N(C\C=C\C1=CC(C(N)=N)=C(F)C=C1)C1=CC=C(OC2CCN(CC2)C(C)=N)C=C1

InChIKey=XBRZJKHVHWAZHK-DQZMXOHWSA-N

C27H36Cl2FN5O5S

632.57

Organic compounds

Benzenoids

Benzene and substituted derivatives

Sulfanilides

Not available

Sulfanilides

Styrenes Phenoxy compounds Phenol ethers Alkyl aryl ethers Fluorobenzenes Piperidines Organosulfonamides Organic sulfonamides Aryl fluorides Aminosulfonyl compounds Carboxylic acid esters Monocarboxylic acids and derivatives Azacyclic compounds Carboxamidines Carboximidamides Hydrocarbon derivatives Carbonyl compounds Hydrochlorides Organic oxides Organofluorides Organopnictogen compounds

Aromatic heteromonocyclic compounds

Sulfanilide - Phenoxy compound - Styrene - Phenol ether - Alkyl aryl ether - Fluorobenzene - Halobenzene - Aryl fluoride - Organic sulfonic acid amide - Organosulfonic acid amide - Aryl halide - Piperidine - Sulfonyl - Aminosulfonyl compound - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Carboxylic acid ester - Amidine - Carboxylic acid amidine - Carboxylic acid derivative - Ether - Azacycle - Monocarboxylic acid or derivatives - Organoheterocyclic compound - Carboximidamide - Carbonyl group - Organopnictogen compound - Hydrocarbon derivative - Organic oxygen compound - Organic oxide - Organohalogen compound - Organofluoride - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Hydrochloride - Organic nitrogen 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