Compound Identification
SMILES
CC1=CC=C(C=C1)S(=O)(=O)N1CC\C=C(Br)/C(=O)C2=CC=CC=C12
InChIKey
InChIKey=LSTOUBIKVMZENT-OMCISZLKSA-N
Formula
C18H16BrNO3S
Mass
406.29
Taxonomic Classification
Taxonomy Tree
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Kingdom
Organic compounds
-
Superclass
Benzenoids
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Class
Benzene and substituted derivatives
-
Subclass
Toluenes
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Level 5
Tosyl compounds
- Level 6 P-toluenesulfonamides
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Level 5
Tosyl compounds
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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
Benzazocines Benzenesulfonamides Benzenesulfonyl compounds Aryl ketones Organosulfonamides Vinylogous amides Sulfonyls Alpha-haloketones Vinyl bromides Bromoalkenes Azacyclic compounds Organonitrogen compounds Organobromides Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
N,n-disubstituted p-toluenesulfonamide - Benzazocine - Benzenesulfonamide - Benzenesulfonyl group - Aryl ketone - Organosulfonic acid amide - Organosulfonic acid or derivatives - Alpha-haloketone - Vinylogous amide - Sulfonyl - Organic sulfonic acid or derivatives - Ketone - Azacycle - Bromoalkene - Haloalkene - Organoheterocyclic compound - Vinyl halide - Vinyl bromide - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organobromide - Organohalogen compound - Organic oxygen 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