Structure Information
Structure

Compound Identification

SMILES

COC1=CC=C(C=C1)N(CC(=O)NN=CC1=CC=C(OCC(=O)NC2=CC=CC=C2OC)C=C1)S(=O)(=O)C1=CC(=C(C)C=C1)[N+]([O-])=O

InChIKey

InChIKey=PWUDHJZEGWEDCQ-UHFFFAOYSA-N

Formula

C32H31N5O9S

Mass

661.69

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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 homomonocyclic compounds

Substituents

N,n-disubstituted p-toluenesulfonamide - Alpha-amino acid or derivatives - Benzenesulfonamide - Sulfanilide - Nitrobenzene - Anilide - Methoxyaniline - Nitrotoluene - Benzenesulfonyl group - Methoxybenzene - Phenoxy compound - Anisole - Phenol ether - N-arylamide - Nitroaromatic compound - Alkyl aryl ether - Organosulfonic acid amide - Aminosulfonyl compound - Sulfonyl - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Organic nitro compound - Carboxamide group - C-nitro compound - Secondary carboxylic acid amide - Carboxylic acid derivative - Ether - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Organic oxoazanium - Allyl-type 1,3-dipolar organic compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organic salt - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Carbonyl group - Organic zwitterion - Aromatic homomonocyclic 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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