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About This Item
Linear Formula:
CF3C6H4CH2OH
CAS Number:
Molecular Weight:
176.14
Beilstein/REAXYS Number:
1450174
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
Recommended Products
assay
98%
refractive index
n20/D 1.459 (lit.)
bp
78-80 °C/4 mmHg (lit.)
density
1.286 g/mL at 25 °C (lit.)
SMILES string
OCc1ccc(cc1)C(F)(F)F
InChI
1S/C8H7F3O/c9-8(10,11)7-3-1-6(5-12)2-4-7/h1-4,12H,5H2
InChI key
MOOUWXDQAUXZRG-UHFFFAOYSA-N
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General description
Photocatalytic oxidation of 4-(trifluoromethyl)benzyl alcohol to corresponding aldehydes on TiO2 photocatalyst under O2 atmosphere has been reported.
Application
4-(Trifluoromethyl)benzyl alcohol was used:
- in the synthesis of highly electron-poor fluorine-containing alkenes
- as a reagent in kinetic studies of phosphonoformate prodrugs and aquachromium (IV)
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
10 - Combustible liquids
wgk_germany
WGK 3
flash_point_f
213.8 °F - closed cup
flash_point_c
101 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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Journal of the American Chemical Society, 114, 4205-4205 (1992)
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One-pot synthesis of fluorine-containing alkenes from in situ-generated stabilized phosphorus ylides.
Pakravan P, et al.
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D C Anderson et al.
Biochemistry, 19(24), 5486-5493 (1980-11-25)
The interactions of horse liver alcohol dehydrogenase (LADH) with the rho-trifluoromethyl derivatives of benzyl alcohol, benzaldehyde, and benzoic acid have been investigated by use of 19F nuclear magnetic resonance. The aldehyde and alcohol are good substrates for the enzyme and
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