Structure Information
Structure

Compound Identification

SMILES

CCN(CC)S(=O)(=O)C1=CC(NC(=O)CSC2=NN=C(N2CC2=CC3=C(OCO3)C=C2)C2=CC=CC=C2)=C(C)C=C1

InChIKey

InChIKey=RLPJQUSYJVGHJL-UHFFFAOYSA-N

Formula

C29H31N5O5S2

Mass

593.72

Export to:

JSON SDF CSV

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 - Phenyltriazole - Phenyl-1,2,4-triazole - Benzenesulfonamide - Benzodioxole - Benzenesulfonyl group - Anilide - N-arylamide - Aryl thioether - Alkylarylthioether - Organosulfonic acid amide - Triazole - 1,2,4-triazole - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Heteroaromatic compound - Azole - Sulfonyl - Aminosulfonyl compound - Secondary carboxylic acid amide - Carboxamide group - Acetal - Carboxylic acid derivative - Oxacycle - Azacycle - Organoheterocyclic compound - Sulfenyl compound - Thioether - Organooxygen compound - Organonitrogen compound - Organosulfur compound - Hydrocarbon derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Carbonyl group - 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

Previous Back Next