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2,4,5-Trifluorobenzyl alcohol

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2,4,5-Trifluorobenzyl alcohol Basic information

Product Name:
2,4,5-Trifluorobenzyl alcohol
Synonyms:
  • 2,4,5-tifluorobenzenecarbinol
  • 2,4,5-TrifluorobenzeneMethanol
  • 2,4,5-TRIFLUOROBENZYL ALCOHOL
  • (2,4,5-TRIFLUORO-PHENYL)-METHANOL
  • RARECHEM AL BD 0314
  • 2,4,5-Trifluorobenzyl alcohol 97%
  • 2,4,5-Trifluorobenzylalcohol97%
  • 2,4,5-Trifluorobenzyl alcohole
CAS:
144284-25-3
MF:
C7H5F3O
MW:
162.11
EINECS:
642-585-0
Product Categories:
  • Alcohols
  • C7 to C8
  • Oxygen Compounds
  • Benzhydrols, Benzyl & Special Alcohols
  • Alcohol
  • Miscellaneous
Mol File:
144284-25-3.mol
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2,4,5-Trifluorobenzyl alcohol Chemical Properties

Melting point:
24 °C
Boiling point:
201-204 °C (lit.)
Density 
1.4 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.472(lit.)
Flash point:
230 °F
storage temp. 
2-8°C
pka
13.17±0.10(Predicted)
form 
liquid
color 
Clear colourless
CAS DataBase Reference
144284-25-3(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38-36/38
Safety Statements 
26-36/37/39-37
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
29062990

MSDS

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2,4,5-Trifluorobenzyl alcohol Usage And Synthesis

Chemical Properties

White solid

General Description

2,4,5-Trifluorobenzyl alcohol is an aryl fluorinated building block. It is also referred to as (2,4,5-trifluorophenyl)methanol [IUPAC name].

Synthesis

165047-24-5

144284-25-3

GENERAL METHOD: Sodium borohydride (0.28 g, 7.5 mmol) was added to a methanol (10 mL) solution of 2,4,5-trifluorobenzaldehyde (5 mmol) cooled in an ice bath in batches over a period of 20 minutes. The reaction mixture was stirred at room temperature for 30 min. The excess sodium borohydride was quenched by adding ice water. Subsequently, the reaction mixture was concentrated and the residue was dissolved in ethyl acetate and washed twice with deionized water. The organic phase was dried with anhydrous sodium sulfate and concentrated to give 2,4,5-trifluorobenzyl alcohol in 96% yield as a colorless oil. The spectral data of the resulting compound were in agreement with standard samples from commercial sources.

References

[1] European Journal of Medicinal Chemistry, 2011, vol. 46, # 2, p. 721 - 737
[2] Organic and Biomolecular Chemistry, 2014, vol. 12, # 30, p. 5781 - 5788

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