Structure Information
Structure

Compound Identification

SMILES

CC(=O)C1=CC(=CC=C1)N1C(=O)CC(N2CCN(CC2)S(=O)(=O)C2=CC=C(C)C=C2)C1=O

InChIKey

InChIKey=KEJNQZUQZFECBA-UHFFFAOYSA-N

Formula

C23H25N3O5S

Mass

455.53

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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 - Alkyl-phenylketone - 1-phenylpyrrolidine - Alpha-amino acid or derivatives - Benzenesulfonamide - Acetophenone - Phenylketone - Benzenesulfonyl group - Benzoyl - Aryl alkyl ketone - Aryl ketone - N-alkylpiperazine - 1,4-diazinane - Carboxylic acid imide, n-substituted - Piperazine - Pyrrolidone - 2-pyrrolidone - Organosulfonic acid amide - Organic sulfonic acid or derivatives - Pyrrolidine - Pyrrole - Sulfonyl - Organosulfonic acid or derivatives - Carboxylic acid imide - Dicarboximide - Tertiary aliphatic amine - Amino acid or derivatives - Tertiary amine - Ketone - Lactam - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Organooxygen compound - Amine - Carbonyl group - Hydrocarbon derivative - Organosulfur compound - Organic oxide - Organic nitrogen compound - Organonitrogen compound - Organic oxygen 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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