CC1=CC=C(C=C1)S(=O)(=O)N1CCNC2OC(C12)C(=O)NC1CCCC2=C1C=NN2CCO[Si](C)(C)C(C)(C)C

InChIKey=FSKHPULPUQAMCU-UHFFFAOYSA-N

C28H43N5O5SSi

589.83

Organic compounds

Benzenoids

Benzene and substituted derivatives

Toluenes

Tosyl compounds - P-toluenesulfonamides

N,N-disubstituted p-toluenesulfonamides

Benzenesulfonamides Benzenesulfonyl compounds Organosulfonamides Piperazines Trialkylheterosilanes Sulfonyls Heteroaromatic compounds Pyrazoles Silyl ethers Hemiaminals Oxetanes Secondary carboxylic acid amides Organic metalloid salts Azacyclic compounds Oxacyclic compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds

Aromatic heteropolycyclic compounds

N,n-disubstituted p-toluenesulfonamide - Benzenesulfonamide - Benzenesulfonyl group - 1,4-diazinane - Piperazine - Organosulfonic acid amide - Azole - Trialkylheterosilane - Pyrazole - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Heteroaromatic compound - Silyl ether - Hemiaminal - Carboxamide group - Oxetane - Secondary carboxylic acid amide - Carboxylic acid derivative - Oxacycle - Azacycle - Organic metalloid salt - Organoheterocyclic compound - Organoheterosilane - Organooxygen compound - Organonitrogen compound - Organic metalloid moeity - Organosilicon compound - Organic oxygen compound - Organic oxide - Organosulfur compound - Hydrocarbon derivative - Amine - Carbonyl group - Organic nitrogen compound - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as n,n-disubstituted p-toluenesulfonamides. These are p-toluenesulfonamide derivatives in which the sulfonamide moiety is N,N-disubstituted.

Not available