Structure Information
Structure

Compound Identification

SMILES

CC1=NN(C(=O)C1N=NC1=CC=C(C=C1)N(CC1=CC=CC=C1)S(=O)(=O)C1=CC=C(C)C=C1)C1=CC(Cl)=C(C=C1Cl)S(O)(=O)=O

InChIKey

InChIKey=NEIUQZRUOIQCSZ-UHFFFAOYSA-N

Formula

C30H25Cl2N5O6S2

Mass

686.58

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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 - Alpha-amino acid or derivatives - Benzenesulfonamide - Sulfanilide - Benzenesulfonate - Arylsulfonic acid or derivatives - Benzenesulfonyl group - 1-sulfo,2-unsubstituted aromatic compound - 1,4-dichlorobenzene - Chlorobenzene - Halobenzene - Organosulfonic acid amide - Pyrazolinone - Aryl chloride - Aryl halide - Sulfonyl - Organosulfonic acid - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Pyrazoline - Aminosulfonyl compound - Azo compound - Organic 1,3-dipolar compound - Organoheterocyclic compound - Azacycle - Propargyl-type 1,3-dipolar organic compound - Carboxylic acid derivative - Organosulfur compound - Hydrocarbon derivative - Organic nitrogen compound - Carbonyl group - Organic oxide - Organohalogen compound - Organic oxygen compound - Organochloride - 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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