Structure Information
Structure

Compound Identification

SMILES

CCOC(=O)C1=CN(CCF)C2=C(C)C(=C(F)C=C2C1=O)C1=CC2=C(CN(C2)S(=O)(=O)C2=CC=C(C)C=C2)C=C1

InChIKey

InChIKey=NFAGMEVFTORYII-UHFFFAOYSA-N

Formula

C30H28F2N2O5S

Mass

566.62

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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 heteropolycyclic compounds

Substituents

N,n-disubstituted p-toluenesulfonamide - Fluoroquinolone - Haloquinoline - Dihydroquinolone - Benzenesulfonamide - Dihydroquinoline - Quinoline - Benzenesulfonyl group - Isoindoline - Isoindole - Isoindole or derivatives - Pyridine carboxylic acid - Pyridine carboxylic acid or derivatives - Pyridine - Aryl halide - Organosulfonic acid amide - Aryl fluoride - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Heteroaromatic compound - Vinylogous amide - Sulfonyl - Carboxylic acid ester - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Hydrocarbon derivative - Alkyl halide - Alkyl fluoride - Organic oxide - Organic oxygen compound - Organohalogen compound - Organofluoride - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Organic nitrogen 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

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