Identification | Back Directory | [Name]
(S)-(+)-ALPHA-(TRIFLUOROMETHYL)BENZYL ALCOHOL | [CAS]
340-06-7 | [Synonyms]
(+)-PHENYL(TRIFLUOROMETHYL)CARBINOL (S)-2,2,2-TRIFLUORO-1-PHENYL-ETHANOL (1S)-1-Phenyl-2,2,2-trifluoroethanol (1S)-2,2,2-Trifluoro-1-phenyl-ethanol (S)-α-(Trifluoromethyl)benzenemethanol (αS)-α-(Trifluoromethyl)benzenemethanol (S)-(+)-1-PHENYL-2,2,2-TRIFLUOROETHANOL (S)-(+)-2,2,2-TRIFLUORO-1-PHENYLETHANOL (S)-(+)-α-(TRIFLUOROMETHYL)BENZYLALCOHOL (s)-(+)-α-(trifluoromethyl)benzyl alcohol (S)-2,2,2-Trifluoro-1-phenylethanol,99%e.e. (S)-(+)-α-(Trifluoromethyl)benzylAlcohol> (1S)-(+)-1-Phenyl-2,2,2-trifluoroethan-1-ol Benzenemethanol, α-(trifluoromethyl)-, (αS)- (S)-(+)-ALPHA-(TRIFLUOROMETHYL)BENZYL ALCOHOL (alphaS)-alpha-(Trifluoromethyl)benzenemethanol (1S)-(+)-1-Phenyl-2,2,2-trifluoroethan-1-ol 99% (S)-(+)-alpha-(Trifluoromethyl)benzyl alcohol 99% (S)-(+)-ALPHA-(TRIFLUOROMETHYL)BENZYL AL COHOL, 99% (97% EE/GLC) (+)-Phenyl(trifluoromethyl)carbinol, (S)-(+)-1-Phenyl-2,2,2-trifluoroethanol | [EINECS(EC#)]
206-430-7 | [Molecular Formula]
C8H7F3O | [MDL Number]
MFCD00077845 | [MOL File]
340-06-7.mol | [Molecular Weight]
176.14 |
Chemical Properties | Back Directory | [Boiling point ]
73-76 °C9 mm Hg(lit.)
| [density ]
1.3 g/mL at 25 °C(lit.)
| [refractive index ]
n20/D 1.462(lit.)
| [Fp ]
184 °F
| [storage temp. ]
Inert atmosphere,Room Temperature | [form ]
Liquid | [pka]
11.91±0.10(Predicted) | [color ]
Clear colorless to pale yellow | [optical activity]
[α]20/D +31.3±0.5°, neat | [BRN ]
2327547 |
Hazard Information | Back Directory | [Uses]
(S)?-?(+)?-?α-?(Trifluoromethyl)?benzyl Alcohol is used in the synthesis of metal-organic framework compounds which may have mesoporous properties. | [Purification Methods]
Purify the chiral alcohols by fractional distillation preferably in a vacuum. [Morrison & Ridgeway Tetrahedron Lett 573 1969, NMR: Pirkle & Beare J Am Chem Soc 90 6250 1968.] The racemate [340-05-6] has b 52-54o/2mm,57-59o/2mm, 64-65o/5mm, d 4 20 1.293, n D 20 1.457, and the 2-carbobenzoyl derivative has m 137-138o [Mosher et al. J Am Chem Soc 78 4374 1956]. [Beilstein 6 IV 3043.] |
|
|