Structure Information
Structure

Compound Identification

SMILES

CN(C1=C(Cl)C=C(C(O)=O)C(Cl)=C1)S(=O)(=O)C1=CC=C(C)C=C1

InChIKey

InChIKey=BZRDDTKDBGEWSW-UHFFFAOYSA-N

Formula

C15H13Cl2NO4S

Mass

374.23

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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 - 2,5-dichlorobenzoic acid - Halobenzoic acid - 3-halobenzoic acid - 2-halobenzoic acid - Halobenzoic acid or derivatives - 3-halobenzoic acid or derivatives - 2-halobenzoic acid or derivatives - Sulfanilide - Benzenesulfonamide - Benzenesulfonyl group - Benzoic acid - Benzoic acid or derivatives - 1-carboxy-2-haloaromatic compound - 1,4-dichlorobenzene - Benzoyl - Halobenzene - Chlorobenzene - Organosulfonic acid amide - Aryl halide - Aryl chloride - Vinylogous halide - Aminosulfonyl compound - Sulfonyl - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organochloride - Organohalogen compound - 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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