CC1=CC(C)(C)NC(=S)N1C1=CC=CC=C1OS(=O)(=O)C1=CC=CC=C1[N+]([O-])=O

InChIKey=XQYSWZOQJYNAEG-UHFFFAOYSA-N

C19H19N3O5S2

433.5

Organic compounds

Benzenoids

Benzene and substituted derivatives

Benzenesulfonic acids and derivatives

Not available

Benzenesulfonate esters

N-phenylthioureas Arylsulfonic acids and derivatives Benzenesulfonyl compounds Nitrobenzenes Phenoxy compounds Nitroaromatic compounds 2-Thiopyrimidines Pyrimidinethiones Hydropyrimidines Organosulfonic acid esters Sulfonyls Thioureas Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds Organic oxoazanium compounds Organic oxides Organonitrogen compounds Organooxygen compounds Hydrocarbon derivatives Organic salts Organic cations

Aromatic heteromonocyclic compounds

Benzenesulfonate ester - N-phenylthiourea - Arylsulfonic acid or derivatives - Benzenesulfonyl group - Nitrobenzene - Phenoxy compound - Nitroaromatic compound - 2-thiopyrimidine - Thiopyrimidine - Pyrimidinethione - Hydropyrimidine - 1,2,3,4-tetrahydropyrimidine - Pyrimidine - Organosulfonic acid ester - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - C-nitro compound - Thiourea - Organic nitro compound - Organoheterocyclic compound - Azacycle - Organic oxoazanium - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Organic nitrogen compound - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Organosulfur compound - Organic salt - Hydrocarbon derivative - Organic oxide - Organic cation - Aromatic heteromonocyclic compound

This compound belongs to the class of organic compounds known as benzenesulfonate esters. These are arenesulfonate esters that result from the formal condensation of the hydroxy group of an alcohol, enol, phenol or heteroarenol with benzenesulfonic acid.

Not available