Structure Information
Structure

Compound Identification

SMILES

COC1=CC=CC=C1N1CCN(CC1)S(=O)(=O)C1=CC(C(N)=O)=C(C)C=C1

InChIKey

InChIKey=KWHZWRPJKXWWKA-UHFFFAOYSA-N

Formula

C19H23N3O4S

Mass

389.47

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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 - Phenylpiperazine - N-arylpiperazine - Benzenesulfonamide - Aminophenyl ether - Methoxyaniline - Benzamide - Benzenesulfonyl group - O-toluamide - Toluamide - Benzoic acid or derivatives - Phenol ether - Tertiary aliphatic/aromatic amine - Phenoxy compound - Benzoyl - Methoxybenzene - Anisole - Aniline or substituted anilines - Dialkylarylamine - Alkyl aryl ether - 1,4-diazinane - Organosulfonic acid amide - Piperazine - Sulfonyl - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Primary carboxylic acid amide - Amino acid or derivatives - Carboxamide group - Tertiary amine - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Ether - Organosulfur compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Amine - Organonitrogen compound - Organic oxygen 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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