Compound Identification
SMILES
CCOC(=O)N1[C@H](CC)C[C@H](NC2(CC3=CC(=CC(=C3)C(F)(F)F)C(F)(F)F)NOC(CO)=N2)C2=C1C=CC(=C2)C(F)(F)F
InChIKey
InChIKey=XWVNZYGHQWZQDN-SWTGPKDFSA-N
Formula
C27H27F9N4O4
Mass
642.523
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Organoheterocyclic compounds
-
Class
Quinolines and derivatives
- Subclass Hydroquinolines
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Class
Quinolines and derivatives
-
Superclass
Organoheterocyclic compounds
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Quinolines and derivatives
Subclass
Hydroquinolines
Intermediate Tree Nodes
Not available
Direct Parent
Hydroquinolines
Alternative Parents
Trifluoromethylbenzenes Carbamate esters Orthocarboxylic acid derivatives Ortho amides Propargyl-type 1,3-dipolar organic compounds Oxacyclic compounds Azacyclic compounds Primary alcohols Organofluorides Organic oxides Hydrocarbon derivatives Carbonyl compounds Amines Alkyl fluorides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Tetrahydroquinoline - Trifluoromethylbenzene - Monocyclic benzene moiety - Benzenoid - Carbamic acid ester - Ortho amide - Orthocarboxylic acid derivative - Oxacycle - Azacycle - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Primary alcohol - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Organonitrogen compound - Organofluoride - Organohalogen compound - Organic oxygen compound - Carbonyl group - Organic nitrogen compound - Alcohol - Alkyl fluoride - Alkyl halide - Amine - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as hydroquinolines. These are derivatives of quinoline in which in which at least one double bond in the quinoline moiety are reduced by adding two hydrogen atoms.
External Descriptors
Not available