Structure Information
Structure

Compound Identification

SMILES

CC1=CC=C(C=C1)S(=O)(=O)N1CC2=CC=CC=C2CC1C(=O)NC1=C(C=CC(=C1)C(F)(F)F)N1CCCCC1

InChIKey

InChIKey=MQBSLNIVZAVBTL-UHFFFAOYSA-N

Formula

C29H30F3N3O3S

Mass

557.63

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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 - Alpha-amino acid amide - Phenylpiperidine - Alpha-amino acid or derivatives - Trifluoromethylbenzene - 2'-aminoanilide - Benzenesulfonamide - Tetrahydroisoquinoline - Benzenesulfonyl group - Anilide - Aniline or substituted anilines - Dialkylarylamine - N-arylamide - Tertiary aliphatic/aromatic amine - Piperidine - Organosulfonic acid amide - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Tertiary amine - Amino acid or derivatives - Secondary carboxylic acid amide - Carboxamide group - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Organonitrogen compound - Organofluoride - Organohalogen compound - Alkyl halide - Organic nitrogen compound - Carbonyl group - Organic oxide - Alkyl fluoride - Amine - Organic oxygen compound - Organooxygen compound - Organosulfur compound - Hydrocarbon derivative - 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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