CHEBI:50283 - (R)-lavandulol

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name (R)-lavandulol
ChEBI ID CHEBI:50283
ChEBI ASCII Name (R)-lavandulol
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Formula C10H18O
Net Charge 0
Average Mass 154.24932
Monoisotopic Mass 154.13577
InChI InChI=1S/C10H18O/c1-8(2)5-6-10(7-11)9(3)4/h5,10-11H,3,6-7H2,1-2,4H3/t10-/m0/s1
InChIKey CZVXBFUKBZRMKR-JTQLQIEISA-N
SMILES CC(C)=CC[C@@H](CO)C(C)=C
Roles Classification
Biological Role(s): pheromone
A semiochemical used in olfactory communication between organisms of the same species eliciting a change in sexual or social behaviour.
(via lavandulol )
plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
(via lavandulol )
Application(s): fragrance
A substance, extract, or preparation for diffusing or imparting an agreeable or attractive smell.
(via lavandulol )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing (R)-lavandulol (CHEBI:50283) is a lavandulol (CHEBI:50281)
(R)-lavandulol (CHEBI:50283) is enantiomer of (S)-lavandulol (CHEBI:50282)
Incoming (R)-lavandulyl diphosphate (CHEBI:50280) has functional parent (R)-lavandulol (CHEBI:50283)
(S)-lavandulol (CHEBI:50282) is enantiomer of (R)-lavandulol (CHEBI:50283)
IUPAC Name
(2R)-5-methyl-2-(prop-1-en-2-yl)hex-4-en-1-ol
Synonyms Sources
(−)-2-isopropenyl-5-methyl-4-hexen-1-ol ChemIDplus
(−)-lavandulol ChemIDplus
(2R)-5-methyl-2-(1-methylethenyl)hex-4-en-1-ol IUPAC
(R)-(−)-lavandulol ChemIDplus
(R)-5-methyl-2-(1-methylethenyl)-4-hexen-1-ol ChemIDplus
(R)-lavandulol UniProt
Registry Numbers Types Sources
1722732 Beilstein Registry Number Beilstein
498-16-8 CAS Registry Number ChemIDplus
Last Modified
21 June 2019