Compound Identification
SMILES
CC(=O)O[C@@H]1C[C@H]2C(C)(C)[C@H](OC(C)=O)[C@H](O)[C@H](OC(=O)C3=CC=CC=C3)[C@]2(C)[C@H]2[C@H](OC(=O)C3=CC=CC=C3)[C@H](C=C)[C@](C)(O)C(=O)[C@]12O
InChIKey
InChIKey=HTQXQVMIWWLNLG-MYFRPNQSSA-N
Formula
C38H44O12
Mass
692.758
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Benzenoids
-
Class
Phenanthrenes and derivatives
- Subclass Hydrophenanthrenes
-
Class
Phenanthrenes and derivatives
-
Superclass
Benzenoids
Kingdom
Organic compounds
Superclass
Benzenoids
Class
Phenanthrenes and derivatives
Subclass
Hydrophenanthrenes
Intermediate Tree Nodes
Not available
Direct Parent
Hydrophenanthrenes
Alternative Parents
Tetracarboxylic acids and derivatives Benzoic acid esters Benzoyl derivatives Cyclitols and derivatives Acyloins Tertiary alcohols Secondary alcohols Ketones Carboxylic acid esters Polyols Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic homopolycyclic compounds
Substituents
Hydrophenanthrene - Tetracarboxylic acid or derivatives - Benzoate ester - Benzoic acid or derivatives - Benzoyl - Acyloin - Cyclitol or derivatives - Monocyclic benzene moiety - Tertiary alcohol - Cyclic alcohol - Carboxylic acid ester - Secondary alcohol - Ketone - Carboxylic acid derivative - Polyol - Alcohol - Carbonyl group - Organic oxygen compound - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Aromatic homopolycyclic compound
Description
This compound belongs to the class of organic compounds known as hydrophenanthrenes. These are a phenanthrene derivative where at least one ring CC bond is substituted by hydrogenation.
External Descriptors
Not available