2,4,5-Trifluorobenzyl alcohol
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
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)
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
- Language:English Provider:SigmaAldrich
- Language:English Provider:ALFA
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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2,4,5-Trifluorobenzyl alcohol(144284-25-3)Related Product Information
- 4-Fluorobenzaldehyde
- Transfluthrin
- 4-Nitrobenzyl alcohol
- Ethyl acetate
- Florfenicol
- Benzyl alcohol
- 4-Trifluoromethylbenzyl chloride
- 2-Hydroxybenzyl alcohol
- Haloperidol
- 3-Fluorobenzyl alcohol
- 4-Fluorobenzonitrile
- 2,4,5-Trifluorobenzoic acid
- 2,3,4,5,6-Pentafluorobenzyl alcohol
- Tetrafluorophthalic anhydride
- DECAFLUOROBENZHYDROL
- Tetrafluorophthalic acid
- 2,3,4,6-TETRAFLUOROBENZOIC ACID
- 2-(PENTAFLUOROPHENYL)-2-PROPANOL