Structure Information
Structure

Compound Identification

SMILES

CC1=CC=C(C=C1)S(=O)(=O)N(CCCN1C(=O)C2=CC=CC=C2C1=O)CC1=C(C)C(CN(CCCN2C(=O)C3=CC=CC=C3C2=O)S(=O)(=O)C2=CC=C(C)C=C2)=C(C)C(CN(CCCN2C(=O)C3=CC=CC=C3C2=O)S(=O)(=O)C2=CC=C(C)C=C2)=C1C

InChIKey

InChIKey=YESLFVKNHPTTOS-UHFFFAOYSA-N

Formula

C66H66N6O12S3

Mass

1231.46

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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 heteropolycyclic compounds

Substituents

N,n-disubstituted p-toluenesulfonamide - Phthalimide - Benzenesulfonamide - Isoindolone - Isoindoline - Isoindole - Benzenesulfonyl group - Isoindole or derivatives - Carboxylic acid imide, n-substituted - Organosulfonic acid amide - Carboxylic acid imide - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Aminosulfonyl compound - Sulfonyl - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organosulfur compound - Organic nitrogen compound - Organic oxygen compound - Aromatic heteropolycyclic 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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