Structure Information
Structure

Compound Identification

SMILES

CN(CC(=O)NNC(=O)C1=CC(=C(SC2=CC=C(C)C=C2)C=C1)[N+]([O-])=O)S(=O)(=O)C1=CC=C(C)C=C1

InChIKey

InChIKey=KACZLEMGMQVGEV-UHFFFAOYSA-N

Formula

C24H24N4O6S2

Mass

528.6

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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 homomonocyclic compounds

Substituents

N,n-disubstituted p-toluenesulfonamide - Diarylthioether - P-sulfanylbenzoic acid or derivatives - Benzenesulfonamide - Alpha-amino acid or derivatives - Nitrobenzene - Benzoic acid or derivatives - Aryl thioether - Nitroaromatic compound - Thiophenol ether - Benzoyl - Diacylhydrazine - Sulfonyl - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Organic nitro compound - Thioenolether - C-nitro compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Sulfenyl compound - Thioether - Organic oxoazanium - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organic zwitterion - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organic hyponitrite - Aromatic homomonocyclic 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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