Compound Identification
SMILES
CC1(C)O[C@@]2(O[C@@H]3C(=C)CC[C@H](Cl)C3(C)C)C(=O)C3=CC(O)=CC(O)=C3C(=O)C2=C[C@H]1Cl
InChIKey
InChIKey=IIQDOCHDDGPWEN-LKMOQRQYSA-N
Formula
C24H26Cl2O6
Mass
481.37
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Organoheterocyclic compounds
-
Class
Naphthopyrans
- Subclass Naphthopyranones
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Class
Naphthopyrans
-
Superclass
Organoheterocyclic compounds
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Naphthopyrans
Subclass
Naphthopyranones
Intermediate Tree Nodes
Not available
Direct Parent
Naphthopyranones
Alternative Parents
Naphthoquinones Tetralins Quinones Aryl alkyl ketones Pyranones and derivatives Ketals 1-hydroxy-4-unsubstituted benzenoids 1-hydroxy-2-unsubstituted benzenoids Vinylogous acids Oxacyclic compounds Organochlorides Organic oxides Hydrocarbon derivatives Alkyl chlorides Aldehydes
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Naphthopyranone - Naphthoquinone - Naphthalene - Tetralin - Quinone - Aryl alkyl ketone - Aryl ketone - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Ketal - Pyranone - Pyran - Benzenoid - Vinylogous acid - Ketone - Acetal - Oxacycle - Organooxygen compound - Organochloride - Organohalogen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Alkyl halide - Alkyl chloride - Aldehyde - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as naphthopyranones. These are compounds containing a naphthopyran skeleton where a ring carbon bears a carboxylic acid group. Naphthtopyran is made up of the pyran ring fused to a naphthalene ring system.
External Descriptors
Not available