Compound Identification
SMILES
CO[C@@H](C=C)[C@H](O)CC1=C(C)C(CC1=O)OC(=O)[C@@H]1[C@@H](\C=C(/C)C(=O)OC)C1(C)C
InChIKey
InChIKey=PBEGFEZPDVLLBH-APSRRMGJSA-N
Formula
C23H32O7
Mass
420.502
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Lipids and lipid-like molecules
-
Class
Fatty Acyls
-
Subclass
Fatty acid esters
-
Level 5
Pyrethroids
- Level 6 Pyrethrins
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Level 5
Pyrethroids
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Subclass
Fatty acid esters
-
Class
Fatty Acyls
-
Superclass
Lipids and lipid-like molecules
Kingdom
Organic compounds
Superclass
Lipids and lipid-like molecules
Class
Fatty Acyls
Subclass
Fatty acid esters
Intermediate Tree Nodes
Pyrethroids
Direct Parent
Pyrethrins
Alternative Parents
Monocyclic monoterpenoids Carbocyclic fatty acids Hydroxy fatty acids Dicarboxylic acids and derivatives Cyclopropanecarboxylic acids and derivatives Methyl esters Enoate esters Secondary alcohols Cyclic ketones Dialkyl ethers Organic oxides Hydrocarbon derivatives
Molecular Framework
Aliphatic homomonocyclic compounds
Substituents
Pyrethrin-backbone - Monocyclic monoterpenoid - Monoterpenoid - Carbocyclic fatty acid - Hydroxy fatty acid - Cyclopropanecarboxylic acid or derivatives - Dicarboxylic acid or derivatives - Enoate ester - Alpha,beta-unsaturated carboxylic ester - Methyl ester - Secondary alcohol - Cyclic ketone - Ketone - Carboxylic acid ester - Carboxylic acid derivative - Ether - Dialkyl ether - Organooxygen compound - Alcohol - Organic oxide - Carbonyl group - Organic oxygen compound - Hydrocarbon derivative - Aliphatic homomonocyclic compound
Description
This compound belongs to the class of organic compounds known as pyrethrins. These are pyrethroids with a structure based on a skeleton that is characterized by the presence of a chrysanthemic acid esterified with a cyclopentenone derivative.
External Descriptors
Not available