Compound Identification
SMILES
NC(=O)C1=CC=CN(C1)NC1=CC(Cl)=CC=C1
InChIKey
InChIKey=OWLJFADHVWHGPG-UHFFFAOYSA-N
Formula
C12H12ClN3O
Mass
249.7
Taxonomic Classification
Taxonomy Tree
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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
Phenylhydrazines Dihydropyridines Chlorobenzenes Aryl chlorides Primary carboxylic acid amides Azacyclic compounds Alkylhydrazines Organochlorides Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
N-substituted nicotinamide - Phenylhydrazine - Chlorobenzene - Dihydropyridine - Halobenzene - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Benzenoid - Hydropyridine - Carboxamide group - Primary carboxylic acid amide - Alkylhydrazine - Carboxylic acid derivative - Azacycle - Hydrazine derivative - Organooxygen compound - Organic oxygen compound - Hydrocarbon derivative - Organic nitrogen compound - Organic oxide - Carbonyl group - Organonitrogen compound - Organochloride - Organohalogen compound - Aromatic 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