Zingiberene

Zingiberene^[1]

Names
IUPAC name 2-Methyl-5-(6-methylhept-5-en-2-yl)cyclohexa-1,3-diene
Identifiers
CAS Number	495-60-3 N
3D model (Jmol)	Interactive image
3DMet	B03248
Beilstein Reference	2554989
ChEBI	CHEBI:10115 Y
ChEMBL	ChEMBL479020 N
ChemSpider	83751 Y
ECHA InfoCard	100.007.096
EC Number	207-804-2
MeSH	zingiberene
PubChem	92776
InChI InChI=1S/C15H24/c1-12(2)6-5-7-14(4)15-10-8-13(3)9-11-15/h6,8-10,14-15H,5,7,11H2,1-4H3/t14-,15+/m0/s1 Y Key: KKOXKGNSUHTUBV-LSDHHAIUSA-N Y Key: KKOXKGNSUHTUBV-LSDHHAIUBW
SMILES C[C@@H](CCC=C(C)C)[C@H]1CC=C(C)C=C1
Properties
Chemical formula	C15H24
Molar mass	204.36 g·mol−1
Density	871.3 mg cm−3 (at 20 °C)
Boiling point	134 to 135 °C (273 to 275 °F; 407 to 408 K) at 2.0 kPa
log P	6.375
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YN ?)
Infobox references

Zingiberene is a monocyclic sesquiterpene that is the predominant constituent of the oil of ginger (Zingiber officinale),^[1][2] from which it gets its name. It can contribute up to 30% of the essential oils in ginger rhizomes. This is the compound that gives ginger its distinct flavoring.

Biosynthesis

Zingiberene is formed in the isoprenoid pathway from farnesyl pyrophosphate (FPP). FPP undergoes a rearrangement to give nerolidyl diphosphate. After the removal of pyrophosphate, the ring closes leaving a carbocation on the tertiary carbon attached to the ring. A 1,3-hydride shift then takes place to give a more stable allylic carbocation. The final step in the formation of zingiberene is the removal of the cyclic allylic proton and consequent formation of a double bond. Zingiberene synthase is the enzyme responsible for catalyzing the reaction forming zingiberene as well as other mono- and sesquiterpenes.^[3]

Biosynthesis of zingiberene

References