(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

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
  • 1,5-Bis(difluoromethyl)naphthalene
  • Phenol, 2-amino-, 1-benzoate
  • N-(4-methylthiazol-2-yl)-5-phenyloxazole-2-carboxamide
  • N-(3-bromophenyl)-5-phenyloxazole-2-carboxamide
  • 5-Amino-3-(4-aminophenyl)-N-methyl-1H-1,2,4-triazole-1-carbothioamide
  • 2-[3-(methylsulfanyl)-5-(4-pyridinyl)-4H-1,2,4-triazol-4-yl]ethanol
  • (3,4-dihydroisoquinolin-2(1H)-yl)(5-(4-methoxyphenyl)oxazol-2-yl)methanone
  • 5-(4-methoxyphenyl)-N-(thiophen-2-ylmethyl)oxazole-2-carboxamide
  • N-(2,4-difluorophenyl)-5-(4-methoxyphenyl)oxazole-2-carboxamide
  • Methyl 4-(5-(4-methoxyphenyl)oxazole-2-carboxamido)benzoate
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