Identification | More | [Name]
2,4-BIS(TRIFLUOROMETHYL)BENZYL ALCOHOL | [CAS]
143158-15-0 | [Synonyms]
2,4-BIS(TRIFLUOROMETHYL)BENZYL ALCOHOL 2,4-DI(TRIFLUOROMETHYL)BENZYL ALCOHOL RARECHEM AL BD 0344 2,4-Bis(trifluoromethyl)benzyl alcohol 98% 2,4-Bis(trifluoromethyl)benzylalcohol98% | [Molecular Formula]
C9H6F6O | [MDL Number]
MFCD00042491 | [Molecular Weight]
244.13 | [MOL File]
143158-15-0.mol |
Safety Data | Back Directory | [Symbol(GHS) ]
 GHS07 | [Signal word ]
Warning | [Hazard statements ]
H315-H319-H335 | [Precautionary statements ]
P261-P280a-P304+P340-P305+P351+P338-P405-P501a | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . S36:Wear suitable protective clothing . | [Hazard Note ]
Irritant | [HazardClass ]
IRRITANT | [HS Code ]
2906290090 |
Hazard Information | Back Directory | [Synthesis]
GENERAL METHOD: Sodium borohydride (0.28 g, 7.5 mmol) was added batchwise to a methanol (10 mL) solution of 2,4-bis(trifluoromethyl)benzaldehyde (5 mmol) cooled in an ice bath over a period of 20 minutes. The reaction mixture was stirred at room temperature for 30 min. Excess sodium borohydride was quenched by addition of ice. 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-bis(trifluoromethyl)benzyl 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 |
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