Structure Information
Structure

Compound Identification

SMILES

COC(=O)C1=CC=C(C=C1)C(N1CCN(CC1)S(=O)(=O)C1=CC=C(C)C=C1)C1=C(N)N(CC(C)C)C(=O)NC1=O

InChIKey

InChIKey=FYIKMBUXHGJFGA-UHFFFAOYSA-N

Formula

C28H35N5O6S

Mass

569.68

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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 - Benzenesulfonamide - Benzoate ester - Benzoic acid or derivatives - Benzenesulfonyl group - Benzoyl - Aminopyrimidine - Aralkylamine - N-alkylpiperazine - Pyrimidone - 1,4-diazinane - Hydropyrimidine - Piperazine - Pyrimidine - Organosulfonic acid amide - Heteroaromatic compound - Vinylogous amide - Methyl ester - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Tertiary amine - Tertiary aliphatic amine - Amino acid or derivatives - Urea - Carboxylic acid ester - Lactam - Carboxylic acid derivative - Organoheterocyclic compound - Azacycle - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Amine - Hydrocarbon derivative - Organosulfur compound - Organic oxygen compound - Primary amine - Organic oxide - 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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