Structure Information
Structure

Compound Identification

SMILES

OS(=O)(=O)C(F)(F)F.CC1=CC=C(C=C1)S(=O)(=O)N1CCCN(CC2=C3SCCSC4=C(C1)C=C(C=C4CN1CC4=CC(=CC5=C4SCCSC4=C(CN(CCCN(C5)S(=O)(=O)C5=CC=C(C)C=C5)S(=O)(=O)C5=CC=C(C)C=C5)C=C(C=C4CN(CC3=CC(=C2)C(C)(C)C)CC2=CC(=CC3=C2SCCSC2=C(CN(CCCN(C3)S(=O)(=O)C3=CC=C(C)C=C3)S(=O)(=O)C3=CC=C(C)C=C3)C=C(C=C2C1)C(C)(C)C)C(C)(C)C)C(C)(C)C)C(C)(C)C)C(C)(C)C)S(=O)(=O)C1=CC=C(C)C=C1

InChIKey

InChIKey=BSGAWFXFVFPAEX-UHFFFAOYSA-N

Formula

C130H163F3N8O15S13

Mass

2551.55

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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

Not available

Substituents

N,n-disubstituted p-toluenesulfonamide - Benzenesulfonamide - Benzenesulfonyl group - Aryl thioether - Trifluoromethanesulfonate - Alkylarylthioether - Aralkylamine - Organosulfonic acid amide - Organosulfonic acid or derivatives - Organosulfonic acid - Organic sulfonic acid or derivatives - Methanesulfonate - Alkanesulfonic acid - Sulfonyl - Tertiary aliphatic amine - Tertiary amine - Trihalomethane - Azacycle - Organoheterocyclic compound - Thioether - Alkyl fluoride - Hydrocarbon derivative - Halomethane - Organic oxide - Organosulfur compound - Organonitrogen compound - Organofluoride - Organohalogen compound - Organic oxygen compound - Organic nitrogen compound - Amine - Alkyl halide - 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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