| Identification | More | [Name]
4-(Trifluoromethyl)benzyl alcohol | [CAS]
349-95-1 | [Synonyms]
4-TRIFLUOROMETHYL BENZENE METHANOL
4-(TRIFLUOROMETHYL)BENZYL ALCOHOL
[4-(TRIFLUOROMETHYL)PHENYL]METHANOL
PTF-BYL
P-(TRIFLUOROMETHYL)BENZYL ALCOHOL
RARECHEM AL BD 0111
Benzenemethanol, 4-(trifluoromethyl)-
4-(trifluoromethyl)benzylic alcohol
4-(Trifluoromethyl)Benzyl
4-(Trifluoromethyl)benzylalcohol97%
p-Trifluoromethylbenzyl alchol
TFMP2O
4-(Trifluoromethyl)benzene-1-methanol | [EINECS(EC#)]
206-494-6 | [Molecular Formula]
C8H7F3O | [MDL Number]
MFCD00004661 | [Molecular Weight]
176.14 | [MOL File]
349-95-1.mol |
| Chemical Properties | Back Directory | [Appearance]
Colorless to light yellow liqui | [Melting point ]
22-25 °C
| [Boiling point ]
78-80 °C/4 mmHg (lit.) | [density ]
1.286 g/mL at 25 °C(lit.)
| [refractive index ]
n20/D 1.459(lit.)
| [Fp ]
213 °F
| [storage temp. ]
Keep in dark place,Sealed in dry,Room Temperature | [form ]
Liquid After Melting | [pka]
13.91±0.10(Predicted) | [color ]
Clear colorless to light brown | [Specific Gravity]
1.286 | [Water Solubility ]
Soluble in water. | [BRN ]
1450174 | [InChI]
InChI=1S/C8H7F3O/c9-8(10,11)7-3-1-6(5-12)2-4-7/h1-4,12H,5H2 | [InChIKey]
MOOUWXDQAUXZRG-UHFFFAOYSA-N | [SMILES]
C1(CO)=CC=C(C(F)(F)F)C=C1 | [CAS DataBase Reference]
349-95-1(CAS DataBase Reference) | [NIST Chemistry Reference]
4-(Trifluoromethyl)benzyl alcohol(349-95-1) |
| Safety Data | Back Directory | [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 .
S37/39:Wear suitable gloves and eye/face protection . | [WGK Germany ]
3
| [F ]
10-23 | [Hazard Note ]
Irritant | [HazardClass ]
CORROSIVE | [HS Code ]
29062900 |
| Hazard Information | Back Directory | [Chemical Properties]
Colorless to light yellow liqui | [Uses]
4-(Trifluoromethyl)benzyl alcohol, is used as a pharmaceutical intermediate, it is also used to predict the NMR spectrum. 4-(Trifluoromethyl)benzyl alcohol is employed as a reagent in, for example, kinetic studies of phosphonoformate prodrugs and aquachromium(IV). | [Definition]
ChEBI: 4-(trifluoromethyl)benzyl alcohol is an aromatic primary alcohol. It is functionally related to a benzyl alcohol. | [Synthesis Reference(s)]
Tetrahedron Letters, 29, p. 4057, 1988 DOI: 10.1016/S0040-4039(00)80416-5 | [General Description]
Photocatalytic oxidation of 4-(trifluoromethyl)benzyl alcohol to corresponding aldehydes on TiO2 photocatalyst under O2 atmosphere has been reported. |
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