Compound Identification
SMILES
CC1=CC=C(C=C1)S(=O)(=O)N1CCN(CC1)C1=NN2C(C=C1)=NN=C2C1=CC=CC=C1
InChIKey
InChIKey=NUCXLRUAMAHFDI-UHFFFAOYSA-N
Formula
C22H22N6O2S
Mass
434.52
Taxonomic Classification
Taxonomy Tree
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Kingdom
Organic compounds
-
Superclass
Benzenoids
-
Class
Benzene and substituted derivatives
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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
N-arylpiperazines Phenyl-1,2,4-triazoles Benzenesulfonamides Triazolopyridazines Benzenesulfonyl compounds Dialkylarylamines Aminopyridazines Organosulfonamides Imidolactams Sulfonyls Heteroaromatic compounds Azacyclic compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
N,n-disubstituted p-toluenesulfonamide - N-arylpiperazine - Phenyl-1,2,4-triazole - Phenyltriazole - Benzenesulfonamide - Benzenesulfonyl group - Triazolopyridazine - Dialkylarylamine - Aminopyridazine - 1,4-diazinane - Piperazine - Pyridazine - Organosulfonic acid amide - Imidolactam - Azole - Heteroaromatic compound - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Triazole - 1,2,4-triazole - Azacycle - Organoheterocyclic compound - Organic nitrogen compound - Hydrocarbon derivative - Organosulfur compound - Amine - Organic oxygen compound - Organic oxide - Organonitrogen 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