Compound Identification
SMILES
CSCCN1C=CCC(=C1)C(N)=O
InChIKey
InChIKey=AFAYJHMYLJVHQP-UHFFFAOYSA-N
Formula
C9H14N2OS
Mass
198.28
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Organoheterocyclic compounds
-
Class
Pyridines and derivatives
-
Subclass
Pyridinecarboxylic acids and derivatives
-
Level 5
Pyridinecarboxamides
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Level 6
Nicotinamides
- Level 7 N-substituted nicotinamides
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Level 6
Nicotinamides
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Level 5
Pyridinecarboxamides
-
Subclass
Pyridinecarboxylic acids and derivatives
-
Class
Pyridines and derivatives
-
Superclass
Organoheterocyclic compounds
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Pyridines and derivatives
Subclass
Pyridinecarboxylic acids and derivatives
Intermediate Tree Nodes
Pyridinecarboxamides - Nicotinamides
Direct Parent
N-substituted nicotinamides
Alternative Parents
Dihydropyridines Vinylogous amides Trialkylamines Primary carboxylic acid amides Amino acids and derivatives Sulfenyl compounds Enamines Dialkylthioethers Azacyclic compounds Allylamines Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aliphatic heteromonocyclic compounds
Substituents
N-substituted nicotinamide - Dihydropyridine - Hydropyridine - Vinylogous amide - Amino acid or derivatives - Carboxamide group - Primary carboxylic acid amide - Tertiary amine - Tertiary aliphatic amine - Allylamine - Azacycle - Carboxylic acid derivative - Enamine - Dialkylthioether - Thioether - Sulfenyl compound - Organic oxide - Organic oxygen compound - Carbonyl group - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Amine - Hydrocarbon derivative - Organic nitrogen compound - Aliphatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as n-substituted nicotinamides. These are nicotnamides in which the pyridine ring is substituted at position 1.
External Descriptors
Not available