CC1=CC=C(C=C1)S(=O)(=O)OC[C@@H](O)[C@H]1ON2O[C@H](C[C@@H]3O[Si](O[C@@H]1[C@H]23)(C(C)(C)C)C(C)(C)C)O[C@H]1CCCC[C@@H]1C1=CC=CC=C1

InChIKey=VKAVTYMBQZUXIL-WWNLRSFNSA-N

C35H51NO9SSi

689.94

Organic compounds

Benzenoids

Benzene and substituted derivatives

Benzenesulfonic acids and derivatives

Not available

Benzenesulfonate esters

p-Methylbenzenesulfonates Tosyl compounds Arylsulfonic acids and derivatives Benzenesulfonyl compounds 1,2-oxazinanes Organosulfonic acid esters Sulfonyls Alkoxysilanes Isoxazolidines Secondary alcohols Oxacyclic compounds Organoheterosilanes N-organohydroxylamines Organic metalloid salts Azacyclic compounds Hydrocarbon derivatives Organic oxides

Aromatic heteropolycyclic compounds

Benzenesulfonate ester - P-methylbenzenesulfonate - Tosyl compound - Arylsulfonic acid or derivatives - Benzenesulfonyl group - Toluene - 1,2-oxazinane - Oxazinane - Organosulfonic acid ester - Organic sulfonic acid or derivatives - Isoxazolidine - Organosulfonic acid or derivatives - Sulfonyl - Alkoxysilane - Secondary alcohol - Organoheterosilane - Organic metalloid salt - N-organohydroxylamine - Azacycle - Oxacycle - Organoheterocyclic compound - Organic nitrogen compound - Organosilicon compound - Hydrocarbon derivative - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organic metalloid moeity - Organic oxide - Organic oxygen compound - Alcohol - Aromatic heteropolycyclic 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