Structure Information
Structure

Compound Identification

SMILES

CC(=O)NC1=C(Cl)C=C(NS(=O)(=O)C2=CC=CC(=C2)C(F)(F)F)C=C1

InChIKey

InChIKey=VSZSKVLDDVWIBS-UHFFFAOYSA-N

Formula

C15H12ClF3N2O3S

Mass

392.78

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Benzenoids

Class

Benzene and substituted derivatives

Subclass

Anilides

Intermediate Tree Nodes

Acetanilides - Haloacetanilides

Direct Parent

O-haloacetanilides

Alternative Parents

Trifluoromethylbenzenes Sulfanilides Benzenesulfonamides N-acetylarylamines Benzenesulfonyl compounds Chlorobenzenes Organosulfonamides Aryl chlorides Acetamides Aminosulfonyl compounds Secondary carboxylic acid amides Carbonyl compounds Hydrocarbon derivatives Organic oxides Organochlorides Alkyl fluorides Organofluorides

Molecular Framework

Aromatic homomonocyclic compounds

Substituents

O-haloacetanilide - Sulfanilide - Trifluoromethylbenzene - Benzenesulfonamide - N-acetylarylamine - Benzenesulfonyl group - N-arylamide - Halobenzene - Chlorobenzene - Aryl chloride - Aryl halide - Organosulfonic acid amide - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Aminosulfonyl compound - Acetamide - Carboxamide group - Secondary carboxylic acid amide - Carboxylic acid derivative - Organonitrogen compound - Organofluoride - Organochloride - Organohalogen compound - Alkyl halide - Hydrocarbon derivative - Alkyl fluoride - Carbonyl group - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Organooxygen compound - Organosulfur compound - Aromatic homomonocyclic compound

Description

This compound belongs to the class of organic compounds known as o-haloacetanilides. These are organic compounds containing an acetamide group conjugated to a phenyl group, which is in turn ortho-substituted with a halogen atom.

External Descriptors

Not available

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