CHEBI:41 - (+)-piperitone

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ChEBI Name (+)-piperitone
ChEBI ID CHEBI:41
Definition The (6S)-enantiomer of piperitone.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C10H16O
Net Charge 0
Average Mass 152.23340
Monoisotopic Mass 152.12012
InChI InChI=1S/C10H16O/c1-7(2)9-5-4-8(3)6-10(9)11/h6-7,9H,4-5H2,1-3H3/t9-/m0/s1
InChIKey YSTPAHQEHQSRJD-VIFPVBQESA-N
SMILES CC(C)[C@@H]1CCC(C)=CC1=O
Roles Classification
Biological Role(s): volatile oil component
Any plant metabolite that is found naturally as a component of a volatile oil.
(via piperitone )
plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
(via piperitone )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing (+)-piperitone (CHEBI:41) is a piperitone (CHEBI:48933)
(+)-piperitone (CHEBI:41) is enantiomer of (−)-piperitone (CHEBI:48934)
Incoming (−)-piperitone (CHEBI:48934) is enantiomer of (+)-piperitone (CHEBI:41)
IUPAC Name
(6S)-3-methyl-6-(propan-2-yl)cyclohex-2-en-1-one
Synonyms Sources
(+)-Piperitone KEGG COMPOUND
(S)-3-methyl-6-(1-methylethyl)-2-cyclohexen-1-one ChemIDplus
(S)-piperitone ChEBI
alpha-Piperitone ChemIDplus
d-Piperitone KEGG COMPOUND
Manual Xrefs Databases
C00003054 KNApSAcK
C09885 KEGG COMPOUND
LMPR0102090024 LIPID MAPS
View more database links
Registry Numbers Types Sources
2042974 Reaxys Registry Number Reaxys
2042974 Beilstein Registry Number Beilstein
6091-50-5 CAS Registry Number KEGG COMPOUND
6091-50-5 CAS Registry Number ChemIDplus
Last Modified
22 January 2015