Fenchol

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Names

[ CAS No. ]:
1632-73-1

[ Name ]:
Fenchol

[Synonym ]:
2-Fenchanol
1,3,3-trimethyl-2-norbornanol
1-Hydroxyfenchane
D-Fenchyl alcohol
fenchyl alcohol
FEMA 2480
FENCHOL
Bicyclo[2.2.1]heptan-2-ol, 1,3,3-trimethyl-
1,3,3-Trimethylbicyclo[2.2.1]heptan-2-ol

Chemical & Physical Properties

[ Density]:
1.0±0.1 g/cm3

[ Boiling Point ]:
202.9±8.0 °C at 760 mmHg

[ Melting Point ]:
35-40ºC

[ Molecular Formula ]:
C10H18O

[ Molecular Weight ]:
154.249

[ Flash Point ]:
73.9±0.0 °C

[ Exact Mass ]:
154.135757

[ PSA ]:
20.23000

[ LogP ]:
2.71

[ Vapour Pressure ]:
0.1±0.9 mmHg at 25°C

[ Index of Refraction ]:
1.502

[ Storage condition ]:
2-8°C

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Hazard Codes ]:
Xi

[ Risk Phrases ]:
36/37/38

[ Safety Phrases ]:
22-24/25-26

[ RIDADR ]:
UN 1325 4.1/PG 2

[ WGK Germany ]:
3

[ RTECS ]:
DT5080000

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

  • Fenchol
  • fenchol
  • fenchol
  • (+)-Fenchol
  • ETHYLFENCHOL
  • 2-ethylfenchol
  • 2-(Methyl(4-oxo-4,5-dihydrothiazol-2-yl)amino)benzoic acid
  • N-[4-(1,3-benzothiazol-2-yl)phenyl]-4-methyl-3-(pyrrolidin-1-ylsulfonyl)benzamide
  • 4-chloro-N-(isoquinolin-5-yl)-3-(pyrrolidin-1-ylsulfonyl)benzamide
  • 4-chloro-N-(isoquinolin-5-yl)-3-(morpholine-4-sulfonyl)benzamide
  • N-[4-(1,3-benzothiazol-2-yl)phenyl]-4-chloro-3-(piperidin-1-ylsulfonyl)benzamide
  • N-(isoquinolin-5-yl)-2-methoxy-5-(piperidin-1-ylsulfonyl)benzamide
  • N-[4-(1,3-benzothiazol-2-yl)phenyl]-2-methoxy-5-(morpholin-4-ylsulfonyl)benzamide
  • N-[4-(1,3-benzothiazol-2-yl)phenyl]-2-methoxy-5-(pyrrolidin-1-ylsulfonyl)benzamide
  • N-(isoquinolin-5-yl)-2-methoxy-5-(morpholin-4-ylsulfonyl)benzamide
  • N-(isoquinolin-5-yl)-2-methoxy-5-(pyrrolidin-1-ylsulfonyl)benzamide
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