Structure Information
Structure

Compound Identification

SMILES

COC1=CC=CC(C=CC(=O)OCC(=O)NC2=C(C)C=CC(=C2)S(=O)(=O)N2CCOCC2)=C1

InChIKey

InChIKey=AAXBCTYHPLYESV-UHFFFAOYSA-N

Formula

C23H26N2O7S

Mass

474.53

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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 - Cinnamic acid ester - Coumaric acid or derivatives - Cinnamic acid or derivatives - Benzenesulfonamide - Anilide - Benzenesulfonyl group - N-arylamide - Styrene - Phenol ether - Phenoxy compound - Methoxybenzene - Anisole - Alkyl aryl ether - Fatty acid ester - Fatty acyl - Organosulfonic acid amide - Morpholine - Oxazinane - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Secondary carboxylic acid amide - Carboxamide group - Carboxylic acid ester - Organoheterocyclic compound - Carboxylic acid derivative - Dialkyl ether - Ether - Oxacycle - Monocarboxylic acid or derivatives - Azacycle - Hydrocarbon derivative - Organic oxide - Organosulfur compound - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Organopnictogen compound - Organonitrogen compound - Organooxygen compound - 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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