Structure Information
Structure

Compound Identification

SMILES

CC[C@H]1C=C(OS(=O)(=O)C(F)(F)F)[C@H](CCCO[Si](C2=CC=CC=C2)(C2=CC=CC=C2)C(C)(C)C)N([C@@H]1CC=C)S(=O)(=O)C1=CC=C(C)C=C1

InChIKey

InChIKey=NWVKWLMBVGRKCQ-OZAKIQRQSA-N

Formula

C37H46F3NO6S2Si

Mass

749.98

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Benzenoids

Class

Benzene and substituted derivatives

Subclass

Toluenes

Intermediate Tree Nodes

Tosyl compounds - P-toluenesulfonamides

Direct Parent

N,N-disubstituted p-toluenesulfonamides

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

N,n-disubstituted p-toluenesulfonamide - Benzenesulfonamide - Benzenesulfonyl group - Trifluoromethanesulfonate - Alkylarylsilane - Hydropyridine - Organosulfonic acid ester - Sulfonic acid ester - Organosulfonic acid amide - Methanesulfonate - Organic sulfonic acid or derivatives - Sulfonyl - Organosulfonic acid or derivatives - Trihalomethane - Silyl ether - Organic metalloid salt - Azacycle - Organoheterosilane - Organoheterocyclic compound - Alkyl fluoride - Organosilicon compound - Hydrocarbon derivative - Halomethane - Organic oxide - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organofluoride - Organic metalloid moeity - Organohalogen compound - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Alkyl halide - Aromatic heteromonocyclic compound

Description

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.

External Descriptors

Not available

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