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2-(Trifluoromethyl)benzyl alcohol

Basic information Safety Supplier Related

2-(Trifluoromethyl)benzyl alcohol Basic information

Product Name:
2-(Trifluoromethyl)benzyl alcohol
Synonyms:
  • 2-(Trifluoromethyl)benzyl alcohol 97%
  • 2-TRIFLUOROBENZYL ALCOHOL
  • 2-(Trifluoromethyl)benzylalcohol97%
  • RARECHEM AL BD 0046
  • OTF-BYL
  • O-(TRIFLUOROMETHYL)BENZYL ALCOHOL
  • 2-(TRIFLUOROMETHYL)BENZYL ALCOHOL
  • 2-TRIFLUOROMETHYL BENZENE METHANOL
CAS:
346-06-5
MF:
C8H7F3O
MW:
176.14
EINECS:
206-467-9
Product Categories:
  • Alcohols
  • C7 to C8
  • Oxygen Compounds
  • Alcohol
  • Benzhydrols, Benzyl & Special Alcohols
Mol File:
346-06-5.mol
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2-(Trifluoromethyl)benzyl alcohol Chemical Properties

Melting point:
4°C
Boiling point:
90 °C20 mm Hg(lit.)
Density 
1.326 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.468(lit.)
Flash point:
198 °F
storage temp. 
Sealed in dry,Room Temperature
form 
clear liquid
pka
14.01±0.10(Predicted)
color 
Colorless to Almost colorless
BRN 
2093714
CAS DataBase Reference
346-06-5(CAS DataBase Reference)
NIST Chemistry Reference
2-(Trifluoromethyl)benzyl alcohol(346-06-5)
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Safety Information

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

MSDS

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2-(Trifluoromethyl)benzyl alcohol Usage And Synthesis

Chemical Properties

Colorless to light yellow liqui

Uses

2-(Trifluoromethyl)benzyl alcohol has been used to investigate the aromatic aldehydes as substrate for yeast alcohol dehydrogenase.

Definition

ChEBI: [2-(Trifluoromethyl)phenyl]methanol is a member of (trifluoromethyl)benzenes.

Synthesis

447-61-0

346-06-5

(1) Water (348.0 g) was added to a 1000 mL three-necked round-bottomed flask equipped with a mechanical stirrer and a thermometer and cooled to 0°C. Subsequently, sodium borohydride (9.5 g, 0.25 mol) was added and stirred for 20 min. Maintaining the temperature at 5 °C, o-trifluoromethylbenzaldehyde (87.1 g, 0.5 mol) was slowly added dropwise. After the dropwise addition, the reaction temperature was maintained at 10 °C for 1 hour. After completion of the reaction, extraction was carried out by adding methyl tert-butyl ether. The organic phases were combined, washed with saturated brine and concentrated under reduced pressure to no fraction to obtain 2-trifluoromethylbenzenemethanol as a colorless transparent liquid with a purity of >99% and a yield of 90%.

References

[1] Patent: CN106588673, 2017, A. Location in patent: Paragraph 0047; 0048
[2] Patent: CN106699729, 2017, A. Location in patent: Paragraph 0066; 0067
[3] Green Chemistry, 2015, vol. 17, # 9, p. 4537 - 4540
[4] Journal of Organic Chemistry, 2017, vol. 82, # 13, p. 6972 - 6977

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