Compound Identification
SMILES
[O-][N+](=O)C1=CN=C2N=CC(C#N)=C(NC3=CC(Cl)=C(F)C=C3)C2=C1
InChIKey
InChIKey=PHJMGNFIXKOHAP-UHFFFAOYSA-N
Formula
C15H7ClFN5O2
Mass
343.7
Taxonomic Classification
Taxonomy Tree
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Kingdom
Organic compounds
-
Superclass
Organoheterocyclic compounds
-
Class
Diazanaphthalenes
- Subclass Naphthyridines
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Class
Diazanaphthalenes
-
Superclass
Organoheterocyclic compounds
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Diazanaphthalenes
Subclass
Naphthyridines
Intermediate Tree Nodes
Not available
Direct Parent
Naphthyridines
Alternative Parents
Aniline and substituted anilines Nitroaromatic compounds Aminopyridines and derivatives Chlorobenzenes Fluorobenzenes Aryl chlorides Aryl fluorides Primary aromatic amines Heteroaromatic compounds Organic oxoazanium compounds Propargyl-type 1,3-dipolar organic compounds Nitriles Secondary amines Azacyclic compounds Organic zwitterions Organic salts Organic oxides Hydrocarbon derivatives Organochlorides Organofluorides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Naphthyridine - Nitroaromatic compound - Aniline or substituted anilines - Aminopyridine - Chlorobenzene - Fluorobenzene - Halobenzene - Aryl chloride - Monocyclic benzene moiety - Primary aromatic amine - Pyridine - Aryl halide - Benzenoid - Aryl fluoride - Heteroaromatic compound - C-nitro compound - Organic nitro compound - Nitrile - Secondary amine - Carbonitrile - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Organic oxoazanium - Azacycle - Cyanide - Organohalogen compound - Organochloride - Organic nitrogen compound - Organofluoride - Amine - Organonitrogen compound - Organic zwitterion - Organic salt - Organic oxygen compound - Hydrocarbon derivative - Organic oxide - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as naphthyridines. These are compounds containing a naphthyridine moiety, a naphthalene in which a carbon atom has been replaced by a nitrogen in each of the two rings. The naphthyridine skeleton can also be described as an assembly two fused pyridine rings, which do not share their nitrogen atom.
External Descriptors
Not available