Basic information Safety Supplier Related

4-Trifluoromethyl-3-fluorobenzyl alcohol

Basic information Safety Supplier Related

4-Trifluoromethyl-3-fluorobenzyl alcohol Basic information

Product Name:
4-Trifluoromethyl-3-fluorobenzyl alcohol
Synonyms:
  • 3-Fluoro-4-(trifluoromethyl)benzenemethanol
  • 2-Fluoro-4-(hydroxymethyl)benzotrifluoride, [3-Fluoro-4-(trifluoromethyl)phenyl]methanol
  • 3-Fluoro-4-(trifluoromethyl)benzylalcohol97%
  • (3-Fluoro-4-(trifluoromethyl)phenyl)methanol
  • 4-Trifluoromethyl-3-fluorob
  • Benzenemethanol, 3-fluoro-4-(trifluoromethyl)-
  • (3-Fluoro-4-(trifluoromethyl)phenyl)meth
CAS:
230295-16-6
MF:
C8H6F4O
MW:
194.13
Product Categories:
  • Fluorine series
Mol File:
230295-16-6.mol
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4-Trifluoromethyl-3-fluorobenzyl alcohol Chemical Properties

Melting point:
28-32°C
Boiling point:
209℃
Density 
1.377
Flash point:
80℃
storage temp. 
Sealed in dry,Room Temperature
pka
13.76±0.10(Predicted)
Appearance
Light green to green Solid-liquid mixture
CAS DataBase Reference
230295-16-6
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Safety Information

HS Code 
2906290090
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4-Trifluoromethyl-3-fluorobenzyl alcohol Usage And Synthesis

Synthesis

204339-72-0

230295-16-6

Step A: Preparation of (3-fluoro-4-(trifluoromethyl)phenyl)methanol: 3-fluoro-4-(trifluoromethyl)benzaldehyde (2.0 g, 10 mmol) and anhydrous methanol (20 mL) were added to a round-bottomed flask fitted with stirring bar. The flask was cooled in an ice bath, followed by the addition of sodium borohydride (0.47 g, 12 mmol) in batches. The ice bath was removed and the reaction mixture was allowed to warm naturally to room temperature. Saturated ammonium chloride solution (2 mL) was added and the mixture was subsequently concentrated under vacuum. The residue was diluted with additional saturated ammonium chloride solution (30 mL) and extracted with ethyl acetate (3 x 30 mL). The organic phases were combined, dried over magnesium sulfate, filtered and concentrated. Yield: 1.8 g (80%). The resulting product was used in the next reaction without further purification.

References

[1] Patent: WO2014/78331, 2014, A1. Location in patent: Paragraph 00855

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