Structure Information
Structure

Compound Identification

SMILES

CC1=CC=C(C=C1)S(=O)(=O)NCC(C1=C(SC=C1)[N+]([O-])=O)S(=O)(=O)OC1=CC=C(C=C1)N(CCCl)CCCl

InChIKey

InChIKey=KRCRMUOIARFOGN-UHFFFAOYSA-N

Formula

C23H25Cl2N3O7S3

Mass

622.55

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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

Direct Parent

P-toluenesulfonamides

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

P-toluenesulfonamide - Benzenesulfonamide - 2-nitrothiophene - Nitrothiophene - Benzenesulfonyl group - Phenoxy compound - Nitroaromatic compound - Nitrogen mustard - Dialkylarylamine - Aniline or substituted anilines - Sulfonic acid ester - Organosulfonic acid amide - Organosulfonic acid ester - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Heteroaromatic compound - Sulfonyl - Thiophene - Aminosulfonyl compound - Organic nitro compound - C-nitro compound - Tertiary amine - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic oxoazanium - Organic zwitterion - Organic oxide - Alkyl chloride - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organochloride - Alkyl halide - Organohalogen compound - Organic oxygen compound - Hydrocarbon derivative - Amine - Organic salt - Organic nitrogen compound - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as p-toluenesulfonamides. These are aromatic heterocyclic compounds containing a toluene that is p-substituted with a sulfonamide group.

External Descriptors

Not available

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