(R)-(-)-TETRAHYDROFURFURYLALCOHOL

[ Density]:
1.038g/cm3

[ Boiling Point ]:
176.8ºC at 760mmHg

[ Molecular Formula ]:
C₅H₁₀O₂

[ Molecular Weight ]:
102.13200

[ Flash Point ]:
83.9ºC

[ Exact Mass ]:
102.06800

[ PSA ]:
29.46000

[ LogP ]:
0.15770

[ Vapour Pressure ]:
0.326mmHg at 25°C

[ Index of Refraction ]:
1.452

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H319

[ Precautionary Statements ]:
P305 + P351 + P338

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

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
R36

[ Safety Phrases ]:
26

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2932190090

[ 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%

Enantioselective synthesis of 4-heterosubstituted cyclopentenones.

J. Org. Chem. 78(8) , 4202-6, (2013)

Racemic 4-hydroxycyclopentenone, readily derived from furfuryl alcohol, can be transformed via its O-Boc derivative to 4-acyloxy, 4-aryloxy-, 4-amino-, or 4-thio-substituted cyclopentenones with high ...

Chemoselective hydrogenolysis of tetrahydrofurfuryl alcohol to 1,5-pentanediol.

Chem. Commun. (Camb.) (15) , 2035-7, (2009)

Direct conversion of tetrahydrofurfuryl alcohol, which is one of the biomass-derived chemicals, to 1,5-pentanediol was realized by chemoselective hydrogenolysis catalyzed by Rh/SiO(2) modified with Re...

[Poisoning with liquid THF-M].

Sud. Med. Ekspert. 24(2) , 23-5, (1981)

More Articles