(-)-Fenchone

Suppliers

Names

[ Name ]:
(-)-Fenchone

[Synonym ]:
(1R,4S)-1,3,3-Trimethylbicyclo[2.2.1]heptan-2-one
EINECS 232-107-5
MFCD00151104
(1R)-(-)-Fenchone
2-Norbornanone, 1,3,3-trimethyl-, (1R,4S)-(+)-
(-)-1,3,3-Trimethyl-2-norbornanone
Bicyclo[2.2.1]heptan-2-one, 1,3,3-trimethyl-, (1R,4S)-
(+)-FENCHONE
(1R,4S)-fenchone

Chemical & Physical Properties

[ Density]:
1.0±0.1 g/cm3

[ Boiling Point ]:
193.5±0.0 °C at 760 mmHg

[ Melting Point ]:
5ºC

[ Molecular Formula ]:
C₁₀H₁₆O

[ Molecular Weight ]:
152.233

[ Flash Point ]:
52.8±0.0 °C

[ Exact Mass ]:
152.120117

[ PSA ]:
17.07000

[ LogP ]:
2.13

[ Vapour Pressure ]:
0.5±0.3 mmHg at 25°C

[ Index of Refraction ]:
1.485

[ Storage condition ]:
Flammables area

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS02

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H226

[ Personal Protective Equipment ]:
Eyeshields;Faceshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Risk Phrases ]:
R10

[ Safety Phrases ]:
S16

[ RIDADR ]:
UN 1224 3/PG 3

[ WGK Germany ]:
3

[ RTECS ]:
RB7875000

[ Packaging Group ]:
III

[ Hazard Class ]:
3.0

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

(+)-Fenchol
(1R,4S)-1,3,3-trimethylbicyclo[2.2.1]heptane-2-one oxime
Bicyclo[2.2.1]heptane, 2-diazo-1,3,3-trimethyl-, (1R,4S)
3-ethynyl-2,2,4-trimethylbicyclo[2.2.1]heptan-3-ol

DownStream

(1S,3R,4R)-2,2,4-trimethyl-3-pyridin-2-ylbicyclo[2.2.1]heptan-3-ol
(+)-2-ethyl fenchol
(+)-Fenchol
(1S,3R,4R)-2,2,4-trimethyl-3-phenylbicyclo[2.2.1]heptan-3-ol

Articles

[Chemical composition of essential oil obtained from Romanian fennel fruits].

Rev. Med. Chir. Soc. Med. Nat. Iasi. 115(2) , 590-4, (2011)

For therapeutical purposes, fennel (Foeniculum vulgare Mill.), an important aromatic plant, is used for its expectorant, antispasmodic, carminative and diuretic properties. The chemical composition, e...

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).

Arch. Biochem. Biophys. 200(2) , 524-33, (1980)

Kinetics and mechanisms of the tropospheric reactions of menthol, borneol, fenchol, camphor, and fenchone with hydroxyl radicals (OH) and chlorine atoms (Cl).

J. Phys. Chem. A 116(16) , 4097-107, (2012)

Relative kinetic techniques have been used to measure the rate coefficients for the reactions of oxygenated terpenes (menthol, borneol, fenchol, camphor, and fenchone) and cyclohexanol with hydroxyl r...

(-)-FENCHONE
(-)-fenchone oxime
fenchone (triphenylphosphoranylidene)hydrazone
1,3,3-Trimethylbicyclo[2.2.1]heptan-2-one
(+/-)-fenchone
D-FENCHONE
2-Ethyl-4-fluoroaniline;hydrochloride
3-Azidopropane-1-sulfinamide
5-(2-azidoethyl)indane
tert-Butyl (2S,3S)-2-(3-bromobenzyl)-3-(2-(dimethylamino)-2-oxoacetamido)pyrrolidine-1-carboxylate
7-bromo-3-(1-methylpiperidin-4-yl)quinazolin-4(3H)-one
5-[4-(Trifluoromethyl)phenoxy]naphthalene-2-carboxylic acid
2-Bromo-6,7-dihydropyrazolo[1,5-a]pyrimidin-5(4H)-one
2-(2,3,4-Trifluorophenyl)prop-2-enoic acid
4-Azido-3-fluoropyridine
2-{[(Tert-butoxy)carbonyl]amino}-5-ethyl-1,3-thiazole-4-carboxylic acid

The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.