Structure Information
Structure

Compound Identification

SMILES

CC(SC1=NN=C(N1C1=CC=CC=C1)C1=C(C)C=CC(=C1)S(=O)(=O)N1CCOCC1)C(=O)C1=CC(F)=C(F)C=C1

InChIKey

InChIKey=JITWEHCIUMSJQD-UHFFFAOYSA-N

Formula

C28H26F2N4O4S2

Mass

584.66

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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 heteromonocyclic compounds

Substituents

N,n-disubstituted p-toluenesulfonamide - Alkyl-phenylketone - Phenyltriazole - Phenyl-1,2,4-triazole - Benzenesulfonamide - Phenylpropane - Phenylketone - Benzenesulfonyl group - Aryl thioether - Benzoyl - Aryl ketone - Aryl alkyl ketone - Fluorobenzene - Halobenzene - Alkylarylthioether - Organosulfonic acid amide - Aryl fluoride - Oxazinane - Aryl halide - Morpholine - 1,2,4-triazole - Triazole - Organic sulfonic acid or derivatives - Sulfonyl - Azole - Heteroaromatic compound - Organosulfonic acid or derivatives - Ketone - Sulfenyl compound - Thioether - Dialkyl ether - Ether - Oxacycle - Azacycle - Organoheterocyclic compound - Organosulfur compound - Aldehyde - Organohalogen compound - Organofluoride - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Aromatic heteromonocyclic 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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