Compound Identification
SMILES
Cl.Cl.CCN(CC1CCN(CC1)C(=O)N1CCCC2=C1C=CC=N2)C(C)CC1=CC(=CC=C1)C(F)(F)F
InChIKey
InChIKey=WITIMBUNLNHTOM-UHFFFAOYSA-N
Formula
C27H37Cl2F3N4O
Mass
561.52
Taxonomic Classification
Taxonomy Tree
-
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
Trifluoromethylbenzenes Amphetamines and derivatives Piperidinecarboxamides Phenylpropanes Aralkylamines Pyridines and derivatives Heteroaromatic compounds Ureas Trialkylamines Azacyclic compounds Hydrocarbon derivatives Hydrochlorides Carbonyl compounds Organic oxides Organofluorides Organopnictogen compounds Alkyl fluorides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Amphetamine or derivatives - Naphthyridine - Trifluoromethylbenzene - Phenylpropane - 1-piperidinecarboxamide - Piperidinecarboxamide - Aralkylamine - Monocyclic benzene moiety - Piperidine - Pyridine - Benzenoid - Heteroaromatic compound - Urea - Tertiary aliphatic amine - Tertiary amine - Azacycle - Amine - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organooxygen compound - Organonitrogen compound - Organofluoride - Organohalogen compound - Organic oxygen compound - Carbonyl group - Alkyl fluoride - Organic nitrogen compound - Alkyl halide - Hydrochloride - 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 These are compounds containing a naphthyridine moiety, a naphthalene in which a carbon atom has been replaced by a nitrogen in each of the two rings.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