Structure Information
Structure

Compound Identification

SMILES

CC1=CC=C(C=C1)S(=O)(=O)N(CCCN(CCCN(CCCN1C(=O)C2=CC=CC=C2C1=O)S(=O)(=O)C1=CC=C(C)C=C1)CC1=CC=CC=C1)CCCN1C(=O)C2=CC=CC=C2C1=O

InChIKey

InChIKey=XMIUQOIDZWPTJK-UHFFFAOYSA-N

Formula

C49H53N5O8S2

Mass

904.11

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 - Phthalimide - Benzenesulfonamide - Isoindolone - Isoindoline - Benzenesulfonyl group - Isoindole - Isoindole or derivatives - Benzylamine - Phenylmethylamine - Aralkylamine - Carboxylic acid imide, n-substituted - Organosulfonic acid amide - Aminosulfonyl compound - Carboxylic acid imide - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Tertiary aliphatic amine - Amino acid or derivatives - Tertiary amine - Azacycle - Carboxylic acid derivative - Organoheterocyclic compound - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Amine - Hydrocarbon derivative - Organic oxide - Organic nitrogen compound - Organic oxygen compound - 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