Compound Identification
SMILES
CCCCC[C@H]1O[C@@H]2C3=C([C@H]1[C@@H]1[C@@H](CCCCC)OC=C4C(=O)[C@@H]5O[C@]5(C\C=C(/C)C(=O)OC(C)(C)C)C(=O)[C@@]214)C(=O)[C@@]1(C\C=C(/C)C(=O)OC(C)(C)C)O[C@H]1C3=O
InChIKey
InChIKey=YAGPEFIYBAEBEW-UZFKQOGYSA-N
Formula
C46H60O12
Mass
804.974
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Organoheterocyclic compounds
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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
Naphthalenes Pyranones and derivatives Oxepanes Fatty acid esters Cyclohexenones Oxanes Dicarboxylic acids and derivatives Vinylogous esters Enoate esters Oxacyclic compounds Epoxides Dialkyl ethers Organic oxides Hydrocarbon derivatives Aldehydes
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Naphthopyranone - Naphthalene - Fatty acid ester - Cyclohexenone - Oxepane - Pyranone - Dicarboxylic acid or derivatives - Fatty acyl - Oxane - Pyran - Vinylogous ester - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Ketone - Carboxylic acid ester - Oxacycle - Ether - Oxirane - Dialkyl ether - Carboxylic acid derivative - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Aldehyde - Carbonyl group - Aliphatic 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