Structure Information
Structure

Compound Identification

SMILES

COC1=C(NS(=O)(=O)C2=CC=C(NC(=O)CN(C3=CC(Cl)=C(Cl)C=C3)S(=O)(=O)C3=CC=C(C)C=C3)C=C2)C=C(C)C=C1

InChIKey

InChIKey=COPVGEDUZOKHKR-UHFFFAOYSA-N

Formula

C29H27Cl2N3O6S2

Mass

648.57

Export to:

JSON SDF CSV

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 - Alpha-amino acid or derivatives - Benzenesulfonamide - Sulfanilide - Anilide - Benzenesulfonyl group - Methoxyaniline - Anisole - Phenoxy compound - 1,2-dichlorobenzene - Phenol ether - N-arylamide - Methoxybenzene - Chlorobenzene - Halobenzene - Alkyl aryl ether - Organosulfonic acid amide - Aryl halide - Aryl chloride - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Aminosulfonyl compound - Sulfonyl - Secondary carboxylic acid amide - Carboxamide group - Carboxylic acid derivative - Ether - Organic oxygen compound - Organohalogen compound - Organochloride - Organonitrogen compound - Carbonyl group - Organic nitrogen compound - Organooxygen compound - Organosulfur compound - Organic oxide - Hydrocarbon derivative - 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

Previous Back Next