(+)-Fenchol

Suppliers

Names

[ CAS No. ]:
2217-02-9

[ Name ]:
(+)-Fenchol

[Synonym ]:
EINECS 216-639-5
1,3,3-trimethyl-2-norbornanol
MFCD00003760
(+)-Fenchol

Chemical & Physical Properties

[ Density]:
0.992g/cm3

[ Boiling Point ]:
201ºC

[ Melting Point ]:
39-45ºC

[ Molecular Formula ]:
C10H18O

[ Molecular Weight ]:
154.24900

[ Flash Point ]:
165 °F

[ Exact Mass ]:
154.13600

[ PSA ]:
20.23000

[ LogP ]:
2.19350

[ Vapour Pressure ]:
0.0693mmHg at 25°C

[ Index of Refraction ]:
1.502

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Risk Phrases ]:
36/38

[ Safety Phrases ]:
S22-S24/25

[ RIDADR ]:
UN 1325 4.1/PG 2

[ WGK Germany ]:
3

Precursor & DownStream

Precursor

DownStream

  • (-)-Fenchone
  • Menthol
  • camphenilone
  • alpha-fenchene
  • 7,7-DIMETHYLBICYCLO[2.2.1] HEPTANE-2,3-DIONE

Articles

Chocolate smells pink and stripy: Exploring olfactory-visual synesthesia.

Cogn Neurosci 6 , 77-88, (2015)

Odors are often difficult to identify, and can be perceived either via the nose or mouth ("flavor"; not usually perceived as a "smell"). These features provide a unique opportunity to contrast concept...

[GC-MS analysis and inhibitory activity of the essential oil extracted from the leaves of Lindera communis].

Zhong Yao Cai 22(3) , 128-31, (1999)

The essential oil isolated from the dried leaves of Lindera communis was analyzed by means of gas chromatography-mass(GC-MS) technique, the structures of 23 chemical components were identified from it...

Biosynthesis of monoterpenes. Enantioselectivity in the enzymatic cyclization of linalyl pyrophosphate to (-)-endo-fenchol.

J. Biol. Chem. 260(26) , 13901-8, (1985)

The conversion of geranyl pyrophosphate to (-)-endo-fenchol is considered to proceed by the initial isomerization of the substrate to (-)-(3R)-linalyl pyrophosphate and the subsequent cyclization of t...


More Articles

Related Compounds

  • (+)-2-ethyl fenchol
  • (+)-5-methylcyclohex-2-en-1-one
  • (+/-)-3,4-epoxytetrahydropyran
  • (+)-Metamfetamine hydrochloride
  • (+)-2,3,4,6-tetrahydro-9-methoxy-1,2,5-trimethyl-1H-pyrido[4,3-b]carbazole
  • (+/-)-N-carbobenzoxy-3-(1,3-dithian-2-yl)-3-(3,4-(methylenedioxy)phenyl)propylamine
  • Methyl 6-[[4-[[[5-(2-fluorophenyl)-3-pyridinyl]amino]carbonyl]-2-pyridinyl]amino]-2-pyridinecarboxylate
  • 2,4-Dichloro-7-cyclohexylmethyl-7H-pyrrolo[2,3-d]pyrimidine
  • 2-[(5-Bromo-2-pyridinyl)amino]-N-(4-phenyl-3-pyridinyl)-4-pyridinecarboxamide
  • 1-(3-Aminopyridin-4-yl)cyclohexanol
  • (4-Chloronaphthalen-2-yl)methanol
  • 1-Propanol, 3-[[2-[4-(methylamino)phenyl]-6-quinolinyl]oxy]-2-[(tetrahydro-2H-pyran-2-yl)oxy]-, 1-(4-methylbenzenesulfonate), (2S)-
  • 4-Amino-2-methylbenzene-1-sulfonyl chloride
  • 4-(Difluoromethyl)-6-iodo-5-methylpyridin-3-ol
  • 4-Bromo-6-hydroxypicolinonitrile
  • 4-bromo-5-methoxy-pyridine-3-carboxylic acid
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