2-(Trifluoromethyl)benzyl alcohol
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
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)
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
- Language:English Provider:2-(Trifluoromethyl)benzyl alcohol
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
- Language:English Provider:ALFA
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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