Compound Identification
SMILES
CC1=CC=C(C=C1)S(=O)(=O)N(CC\C=C\C(=O)C1=CC=CC=C1)CC#C
InChIKey
InChIKey=PLLNUYKTOYRHKQ-YRNVUSSQSA-N
Formula
C21H21NO3S
Mass
367.46
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Benzenoids
-
Class
Benzene and substituted derivatives
-
Subclass
Toluenes
-
Level 5
Tosyl compounds
- Level 6 P-toluenesulfonamides
-
Level 5
Tosyl compounds
-
Subclass
Toluenes
-
Class
Benzene and substituted derivatives
-
Superclass
Benzenoids
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
Benzenesulfonamides Benzenesulfonyl compounds Benzoyl derivatives Aryl ketones Organosulfonamides Enones Aminosulfonyl compounds Acryloyl compounds Acetylides Organonitrogen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic homomonocyclic compounds
Substituents
N,n-disubstituted p-toluenesulfonamide - Benzenesulfonamide - Benzenesulfonyl group - Benzoyl - Aryl ketone - Organosulfonic acid amide - Acryloyl-group - Enone - Organic sulfonic acid or derivatives - Alpha,beta-unsaturated ketone - Aminosulfonyl compound - Sulfonyl - Organosulfonic acid or derivatives - Ketone - Acetylide - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Organic oxide - Organic oxygen compound - Hydrocarbon derivative - 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