Compound Identification
SMILES
CC1=C(C=C(C=C1)S(=O)(=O)N1CC[NH+]2CCCC[C@@H]2C1)[N+]([O-])=O
InChIKey
InChIKey=WYCDMBZQOYLYRN-CYBMUJFWSA-O
Formula
C15H22N3O4S
Mass
340.42
Taxonomic Classification
Taxonomy Tree
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Kingdom
Organic compounds
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Superclass
Benzenoids
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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
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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 Piperazinopiperidines Benzenesulfonyl compounds Nitrobenzenes Nitrotoluenes Nitroaromatic compounds N-alkylpiperazines Hydropyridines Piperidines Organosulfonamides Sulfonyls Quaternary ammonium salts Trialkylamines Azacyclic compounds Organic oxoazanium compounds Organic salts Hydrocarbon derivatives Organic oxides Organic cations
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
N,n-disubstituted p-toluenesulfonamide - Benzenesulfonamide - Piperazino-1,2-a-piperidine - Nitrotoluene - Benzenesulfonyl group - Nitrobenzene - Nitroaromatic compound - N-alkylpiperazine - Organosulfonic acid amide - 1,4-diazinane - Piperidine - Hydropyridine - Piperazine - Quaternary ammonium salt - Organosulfonic acid or derivatives - Sulfonyl - Organic sulfonic acid or derivatives - C-nitro compound - Organic nitro compound - Tertiary aliphatic amine - Organoheterocyclic compound - Azacycle - Organic oxoazanium - Organosulfur compound - Organonitrogen compound - Hydrocarbon derivative - Amine - Organic oxide - Organic oxygen compound - Organic salt - Organic nitrogen compound - Organic cation - 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