(R)-(-)-TETRAHYDROFURFURYLALCOHOL

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Names

[ CAS No. ]:
22415-59-4

[ Name ]:
(R)-(-)-TETRAHYDROFURFURYLALCOHOL

[Synonym ]:
(-)-(R)-tetrahydro-2-furanmethanol
(R)-Tetrahydrofurfuryl alcohol
(R)-2-tetrahydrofuryl methanol
[(2R)-2-oxolanyl]methanol
MFCD03093085
(-)-(R)-tetrahydrofurane-3-methanol
(R)-(Tetrahydrofuran-2-yl)methanol
(R)-Tetrahydrofuran-2-methanol
(R)-(-)-Tetrahydrofurfuryl alcohol
(R)-(-)-Tetrahydrofurfurylalcohol

Chemical & Physical Properties

[ 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

Safety Information

[ 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

Preparation


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

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


Related Compounds

  • (R)-2-Amino-2-(3-fluoro-2-methylphenyl)ethanol hydrochloride
  • (R)-(-)-Hydroxy Chloroquine Diphosphate
  • (R-(R*,R*))-N-(2-Hydroxy-1-(hydroxymethyl)-2-(4-nitrophenyl)ethyl)-2-o xoacetamide
  • (R)-2-aMino-2-(3-(trifluoroMethyl)phenyl)ethanol hydrochloride
  • (R)-2-(2-Chloro-5-(trifluoromethyl)phenyl)pyrrolidine hydrochloride
  • (R)-2-(3-chlorophenyl)piperidine hydrochloride
  • 7-(2-isocyanatoethyl)-1-methyl-1H-indole
  • 4-amino-4-(1H-1,2,4-triazol-3-yl)cyclohexan-1-ol
  • 2-(2-Fluoro-3-nitrophenyl)propan-2-amine
  • 3-(but-3-yn-1-yl)-N-ethylbenzamide
  • 3-({Imidazo[1,2-a]pyridin-2-yl}methyl)piperidin-3-ol
  • 3-(7-Chloro-1,3-dioxaindan-5-yl)butan-1-amine
  • 1-Bromo-4-methyl-2-(prop-2-yn-1-yl)benzene
  • 1-[1-(3,5-Difluoropyridin-4-yl)cyclopropyl]ethan-1-one
  • 4-(aminomethyl)-4-(1-ethyl-1H-1,2,4-triazol-5-yl)cyclohexan-1-ol
  • 2-Amino-5-chloro-4-ethylbenzene-1-sulfonyl fluoride
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