CHEBI:48697 - α-campholenaldehyde

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ChEBI Name α-campholenaldehyde
ChEBI ID CHEBI:48697
ChEBI ASCII Name alpha-campholenaldehyde
Definition An aldehyde that is acetaldehyde in which one of the methyl hydrogens is substituted by a 2,2,3-trimethylcyclopent-3-en-1-yl group. It is a constituent of the essential oil extracted from Angasomyrtus salina.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C10H16O
Net Charge 0
Average Mass 152.23340
Monoisotopic Mass 152.12012
InChI InChI=1S/C10H16O/c1-8-4-5-9(6-7-11)10(8,2)3/h4,7,9H,5-6H2,1-3H3
InChIKey OGCGGWYLHSJRFY-UHFFFAOYSA-N
SMILES [H]C(=O)CC1CC=C(C)C1(C)C
Roles Classification
Biological Role(s): plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
Application(s): fragrance
A substance, extract, or preparation for diffusing or imparting an agreeable or attractive smell.
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ChEBI Ontology
Outgoing α-campholenaldehyde (CHEBI:48697) has functional parent acetaldehyde (CHEBI:15343)
α-campholenaldehyde (CHEBI:48697) has parent hydride cyclopentene (CHEBI:49155)
α-campholenaldehyde (CHEBI:48697) has role fragrance (CHEBI:48318)
α-campholenaldehyde (CHEBI:48697) has role plant metabolite (CHEBI:76924)
α-campholenaldehyde (CHEBI:48697) is a α-CH2-containing aldehyde (CHEBI:73359)
α-campholenaldehyde (CHEBI:48697) is a monocyclic compound (CHEBI:33661)
Incoming 2-(2,2,3-trimethylcyclopent-3-enyl)acrylaldehyde (CHEBI:48713) has functional parent α-campholenaldehyde (CHEBI:48697)
(R)-α-campholenaldehyde (CHEBI:49150) is a α-campholenaldehyde (CHEBI:48697)
IUPAC Name
(2,2,3-trimethylcyclopent-3-en-1-yl)acetaldehyde
Synonyms Sources
2,2,3-trimethyl-3-cyclopentene-1-acetaldehyde ChemIDplus
2,2,3-Trimethylcyclopent-3-en-1-yl acetaldehyde ChemIDplus
2-(2,2,3-trimethylcyclopent-3-en-1-yl)acetaldehyde ChEBI
alpha-Campholenaldehyde ChemIDplus
α-campholenic aldehyde ChEBI
campholenic aldehyde ChEBI
Manual Xrefs Databases
CN101541728 Patent
CN1660746 Patent
US2010004489 Patent
WO02090261 Patent
WO2008017184 Patent
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Registry Numbers Types Sources
1859709 Reaxys Registry Number Reaxys
91819-58-8 CAS Registry Number ChemIDplus
Citation Waiting for Citations Type Source
IND20393379 Agricola citation Europe PMC
Last Modified
03 March 2014