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(4-(Trifluoromethyl)phenyl)methanol

Names

[ CAS No. ]:
349-95-1

[ Name ]:
(4-(Trifluoromethyl)phenyl)methanol

[Synonym ]:
Q1R DXFFF
[4-(Trifluoromethyl)phenyl]methanol
4-(Trifluoromethyl)benzylic alcohol
(4-(Trifluoromethyl)phenyl)methanol
EINECS 206-494-6
3-(trifluoromethyl)benzyl alcohol
4-(Trifluoromethyl)benzyl alcohol
4-trifluoromethylbenzyl alcohol
MFCD00004661
4-(Hydroxymethyl)benzotrifluoride
4-(Trifluoromethyl)benzenemethanol
p-Trifluoromethylbenzyl alcohol
p-(Trifluoromethyl)benzyl alcohol
Benzenemethanol, 4-(trifluoromethyl)-
4-(Trifluoromethyl)benzylalcohol

Chemical & Physical Properties

[ Density]:
1.3±0.1 g/cm3

[ Boiling Point ]:
213.7±0.0 °C at 760 mmHg

[ Melting Point ]:
22-25 °C

[ Molecular Formula ]:
C8H7F3O

[ Molecular Weight ]:
176.136

[ Flash Point ]:
100.6±0.0 °C

[ Exact Mass ]:
176.044907

[ PSA ]:
20.23000

[ LogP ]:
1.61

[ Vapour Pressure ]:
0.1±0.4 mmHg at 25°C

[ Index of Refraction ]:
1.463

MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
Eyeshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
Xi:Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36-S37/39

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
29062900

Synthetic Route

Precursor & DownStream

Customs

[ HS Code ]: 2906299090

[ Summary ]:
2906299090 other aromatic alcohols。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:5.5%。General tariff:30.0%

Articles

Determination of the equilibrium distibution between alcohol and aldehyde substrates when bound to horse liver alcohol dehydrogenase using magnetic resonance.

Biochemistry 19(24) , 5486-93, (1980)

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 mag...

Prochiral selectivity in H(2)O(2)-promoted oxidation of arylalkanols catalysed by chloroperoxidase. The role of the interactions between the OH group and the amino-acid residues in the enzyme active site.

Eur. J. Biochem. 268(3) , 665-72, (2001)

The H(2)O(2)-promoted oxidations of (R)-[alpha-(2)H(1)]-and (S)-[alpha-(2)H(1)]-arylalkanols catalysed by chloroperoxidase (CPO) from Caldariomyces fumago have been investigated. It has been found tha...

J. Chem. Soc., Perkin Trans. II , 1145, (1992)


More Articles


Related Compounds

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