1-(2-FURYL)ETHAN-1-OL

Names

[ Name ]:
1-(2-FURYL)ETHAN-1-OL

[Synonym ]:
DL-1-(2-Furyl)ethanol
MFCD00077775
DL-1-(2-Furyl)ethanol,stabilized
1-furylethanol
EINECS 224-130-4
A-2-FURYLETHANOL

Chemical & Physical Properties

[ Density]:
1.078 g/mL at 20 °C(lit.)

[ Boiling Point ]:
167-170 °C

[ Melting Point ]:
73-74ºC

[ Molecular Formula ]:
C₆H₈O₂

[ Molecular Weight ]:
112.12700

[ Flash Point ]:
34.6ºC

[ Exact Mass ]:
112.05200

[ PSA ]:
33.37000

[ LogP ]:
1.33290

[ Index of Refraction ]:
n20/D 1.479

[ Storage condition ]:
2-8°C

MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S36/37/39-S26-S23

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2932190090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

Furfural
methyl iodide
1-(Furan-2-yl)ethanone
METHYLLITHIUM
Methylmagnesium chloride
trimethylaluminum
1-(2-FURYL)ETHAN-1-OL
DL-1-(2,5-Dimethoxy-2,5-dihydrofuran-2-yl)ethanol
METHYLMAGNESIUM IODIDE

DownStream

Ethyl 4-Oxohexanoate
(3beta,5beta)-3-[(6-deoxy-alpha-L-mannopyranosyl)oxy]-14-hydroxycard-20(22)-enolide
5-Ethylfuran-2-carboxylic acid
Afzelin
4-hydroxy-2-methylcyclopent-2-en-1-one
2-Furancarboxamide
1-(2-FURYL)ETHAN-1-OL
Maltol
Ramnodigin
1-(Furan-2-yl)ethanone

Customs

[ HS Code ]: 2932190090

[ Summary ]:
2932190090 other compounds containing an unfused furan ring (whether or not hydrogenated) in the structure VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:20.0%

Articles

Amino acid-catalyzed formation of 2-vinylfuran from lipid-derived 4-oxo-2-hexenal.

Food Chem. 188 , 591-5, (2015)

The formation of 2-vinylfuran from the corresponding 4-oxo-2-hexenal (OHE, a lipid oxidation product) under the catalysis of amino acid were studied. The effects of amino acids, reaction temperature, ...

Lipase-catalyzed irreversible transesterification of 1-(2-furyl)ethanol using isopropenyl acetate.

Chirality 13(2) , 118-23, (2001)

Asymmetric acetylation of racemic 1-(2-furyl)ethanol with the innocuous acyl donor isopropenyl acetate catalyzed by lipases in organic media afforded the chiral alcohol and acetate in high enantiomeri...

An Enantioselective Total Synthetic Approach to (+)-Heptemerone G and (+)-Guanacastepene A from 2-Furyl Methyl Carbinol. Michalak K and Wicha J.

Synlett 24 , 1387-1390, (2013)