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
6091-50-5 CAS Registry Number KEGG COMPOUND
6091-50-5 CAS Registry Number ChemIDplus
Last Modified
22 January 2015