Compound Identification
SMILES
Cl.Br.COC1=CC2=C(C[C@H]3[C@H]4CCCC[C@@]24CCN3C)C=C1.CN(C)CCCN1C2=CC=CC=C2CCC2=C1C=C(Cl)C=C2
InChIKey
InChIKey=YLSRAKJVZHZSLC-CFKASLMESA-N
Formula
C37H50BrCl2N3O
Mass
703.63
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Alkaloids and derivatives
- Class Morphinans
-
Superclass
Alkaloids and derivatives
Kingdom
Organic compounds
Superclass
Alkaloids and derivatives
Class
Morphinans
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Morphinans
Alternative Parents
Dibenzazepines Phenanthrenes and derivatives Alkyldiarylamines Benzazocines Tetralins Anisoles Alkyl aryl ethers Aralkylamines Azepines Piperidines Aryl chlorides Trialkylamines Azacyclic compounds Hydrochlorides Organochlorides Hydrocarbon derivatives Hydrobromides
Molecular Framework
Not available
Substituents
Morphinan - Dibenzazepine - Phenanthrene - Benzazocine - Alkyldiarylamine - Benzazepine - Tetralin - Anisole - Phenol ether - Tertiary aliphatic/aromatic amine - Aralkylamine - Alkyl aryl ether - Azepine - Benzenoid - Piperidine - Aryl chloride - Aryl halide - Tertiary aliphatic amine - Tertiary amine - Organoheterocyclic compound - Azacycle - Ether - Hydrochloride - Hydrocarbon derivative - Organohalogen compound - Organic oxygen compound - Organic nitrogen compound - Organochloride - Organonitrogen compound - Organooxygen compound - Amine - Hydrobromide - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as morphinans. These are polycyclic compounds with a four-ring skeleton with three condensed six-member rings forming a partially hydrogenated phenanthrene moiety, one of which is aromatic while the two others are alicyclic.
External Descriptors
Not available