CC1=CC=C(C=C1)S(=O)(=O)OC[C@@H]1O[C@@H]1[C@H]1OC(=N[C@H]1CO[Si](C1=CC=CC=C1)(C1=CC=CC=C1)C(C)(C)C)C1=CC=CC=C1

InChIKey=RPJWUXKSOFDSNF-CUPIEXAXSA-N

C36H39NO6SSi

641.85

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 Alkylarylsilanes Organosulfonic acid esters Sulfonyls Oxazolines Silyl ethers Propargyl-type 1,3-dipolar organic compounds Oxacyclic compounds Azacyclic compounds Organoheterosilanes Organic metalloid salts Epoxides Dialkyl ethers Organonitrogen compounds Organic oxides Hydrocarbon derivatives

Aromatic heteromonocyclic compounds

Benzenesulfonate ester - P-methylbenzenesulfonate - Tosyl compound - Arylsulfonic acid or derivatives - Benzenesulfonyl group - Toluene - Alkylarylsilane - Organosulfonic acid ester - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Oxazoline - Silyl ether - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Organoheterocyclic compound - Organic metalloid salt - Azacycle - Oxacycle - Ether - Oxirane - Organoheterosilane - Dialkyl ether - Organic nitrogen compound - Organosilicon compound - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organic metalloid moeity - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - 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