Chemistry:Fenchol
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-endo-(%2B)-Fenchol.svg) (1R)-endo-(+)-Fenchol
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| Names | |
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| IUPAC name
(1R,2R,4S)-1,3,3-Trimethyl-2-norbornanol
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| Other names
Fenchyl alcohol
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| Identifiers | |
3D model (JSmol)
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| ChEMBL | |
PubChem CID
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| UNII | |
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| Properties | |
| C10H18O | |
| Molar mass | 154.253 g·mol−1 |
| Density | 0.942 g/cm3 |
| Melting point | 39 to 45 °C (102 to 113 °F; 312 to 318 K) |
| Boiling point | 201 °C (394 °F; 474 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
 verify (what is   ?)
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| Infobox references | |
Tracking categories (test):
Fenchol or 1,3,3-trimethyl-2-norbornanol is a monoterpenoid and an isomer of borneol. It is a colorless or white solid. It occurs widely in nature.
The naturally occurring enantiomere (1R)-endo-(+)-fenchol is used extensively in perfumery. Fenchol gives basil its characteristic scent,[2][3] and comprises 15.9% of the volatile oils of some species of Aster.[4]
It is biosynthesized from geranyl pyrophosphate via isomerization to linalyl pyrophosphate.[5]
Oxidation of fenchol gives fenchone.
References
- ↑ Datasheet at chemexper.com
- ↑ "FES - (-)-endo-fenchol synthase, chloroplastic precursor - Ocimum basilicum (Sweet basil) - FES gene & protein". https://www.uniprot.org/uniprot/Q5SBP2.
- ↑ Kotan, Recep; Kordali, Saban; Cakir, Ahmet (August 2007). "Screening of antibacterial activities of twenty-one oxygenated monoterpenes". Zeitschrift für Naturforschung C 62 (7–8): 507–513. doi:10.1515/znc-2007-7-808. PMID 17913064.
- ↑ Matasyoh, Josphat C.; Kiplimo, Joyce J.; Karubiu, Nicholas M.; Hailstorks, Tiffany P. (2006). "Chemical composition and antimicrobial activity of essential oil of Tarchonanthus camphoratus". Food Chemistry 101 (3): 1183–1187. doi:10.1016/j.foodchem.2006.03.021.
- ↑ Satterwhite, D. M.; Wheeler, C. J.; Croteau, R. (15 November 1985). "Biosynthesis of monoterpenes. Enantioselectivity in the Enzymatic Cyclization of Linalyl Pyrophosphate to (-)-endo-Fenchol". The Journal of Biological Chemistry 260 (26): 13901–8. doi:10.1016/S0021-9258(17)38661-1. PMID 4055764.
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