Structure Information
Structure

Compound Identification

SMILES

CN(C)S(=O)(=O)C1=CC(NC(=O)COC(=O)[C@H]2CN(C(=O)C2)C2=CC3=C(OCCO3)C=C2)=C(C)C=C1

InChIKey

InChIKey=IIKYGDKDGOUXEV-MRXNPFEDSA-N

Formula

C24H27N3O8S

Mass

517.55

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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 - P-toluenesulfonamides

Direct Parent

N,N-disubstituted p-toluenesulfonamides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

N,n-disubstituted p-toluenesulfonamide - Benzenesulfonamide - Benzo-1,4-dioxane - Benzodioxane - Anilide - Benzenesulfonyl group - Pyrrolidine carboxylic acid or derivatives - N-arylamide - Pyrrolidine carboxylic acid - Oxoproline - Alkyl aryl ether - Pyrrolidone - Organosulfonic acid amide - 2-pyrrolidone - Para-dioxin - Aminosulfonyl compound - Tertiary carboxylic acid amide - Sulfonyl - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Pyrrolidine - Carboxamide group - Carboxylic acid ester - Lactam - Secondary carboxylic acid amide - Monocarboxylic acid or derivatives - Ether - Carboxylic acid derivative - Oxacycle - Azacycle - Organoheterocyclic compound - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Aromatic heteropolycyclic 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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