| Weight | 154.253 g/mol |
|---|---|
| Formula | C10H18O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
Fenchol (512-13-0, 1632-73-1)
fenchyl alcohol · fenchol, ((endo)-(+-))-isomer · fenchol, ((exo)-(+-))-isomer
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- Biosynthesis of monoterpenes: Preliminary characterization of l-endo-fenchol synthetase from fennel (Foeniculum vulgare) and evidence that no free intermediate is involved in the cyclization of geranyl pyrophosphate to the rearranged product (Archives of Biochemistry and Biophysics, 1980)
- Biosynthesis of monoterpenes. Enantioselectivity in the enzymatic cyclization of linalyl pyrophosphate to (-)-endo-fenchol. (Journal of Biological Chemistry, 1985)
- Biosynthesis of monoterpenes: conversion of the acyclic precursors geranyl pyrophosphate and neryl pyrophosphate to the rearranged monoterpenes fenchol and fenchone by a soluble enzyme preparation from fennel (foeniculum vulgare) (Archives of Biochemistry and Biophysics, 1980)
- Monoterpene biosynthesis: Mechanistic evaluation of the geranyl pyrophosphate:()-endo-fenchol cyclase from fennel (Foeniculum vulgare) (Archives of Biochemistry and Biophysics, 1989)
- Enzymic cyclization of [1-18O]geranyl pyrophosphate to l-endo-fenchol (Journal of the American Chemical Society, 1984)
- Biosynthesis of monoterpenes. Stereochemistry of the enzymatic cyclization of geranyl pyrophosphate to (-)-endo-fenchol. (Journal of Biological Chemistry, 1988)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - fenchyl alcohol
- fenchol, ((endo)-(+-))-isomer
- fenchol, ((exo)-(+-))-isomer
- fenchol, (endo)-isomer
- endo-fenchol
- fenchol, (exo)-isomer
- fenchol, (1S-exo)-isomer
- fenchol, (1R-endo)-isomer
- fenchol, (1S-endo)-isomer
- 1,3,3-trimethyl-2-norbornanol
-
SMILESCC1(C2CCC(C2)(C1O)C)C
-
InChIKeyIAIHUHQCLTYTSF-UHFFFAOYSA-N
- Pubchem - Fenchol
- Wikipedia - Fenchol
Fenchol or 1,3,3-trimethyl-2-norbornanol is a terpene and an isomer of borneol. The naturally occurring enantiopure (1R)-endo-(+)-fenchol is used extensively in perfumery. Fenchol is also, a scent from basil.
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Fenchol
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