3-(Trifluoromethyl)phenylboronic acid

Names

[ Name ]:
3-(Trifluoromethyl)phenylboronic acid

[Synonym ]:
α,α,α-Trifluoro-m-tolylboronic Acid
B-[3-(Trifluoromethyl)phenyl]boronic acid
Dihydroxy[3-(trifluoromethyl)phenyl]borane
3-Trifluoromethylphenylboronic acid
MFCD00151854
3-(Trifluoromethyl)benzeneboronic acid
[3-(Trifluoromethyl)phenyl]boronic acid
QBQR CXFFF
α,α,α-Trifluoro-m-tolueneboronic acid
(3-(Trifluoromethyl)phenyl)bo
3-(Trifluoromethyl)phenylboronic acid
Boronic acid, B-[3-(trifluoromethyl)phenyl]-
[3-(Trifluoromethyl)phenyl]boranediol

Biological Activity

[Description]:

3-(Trifluoromethyl)phenylboronic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

[Related Catalog]:

Research Areas >> Others

Signaling Pathways >> Others >> Others

Chemical & Physical Properties

[ Density]:
1.4±0.1 g/cm3

[ Boiling Point ]:
268.2±50.0 °C at 760 mmHg

[ Melting Point ]:
163-166 °C(lit.)

[ Molecular Formula ]:
C₇H₆BF₃O₂

[ Molecular Weight ]:
189.93

[ Flash Point ]:
116.0±30.1 °C

[ Exact Mass ]:
190.041290

[ PSA ]:
40.46000

[ LogP ]:
2.16

[ Vapour Pressure ]:
0.0±0.6 mmHg at 25°C

[ Index of Refraction ]:
1.462

[ Storage condition ]:
0-6°C

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Hazard Codes ]:
Xi:Irritant

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S22-S24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2934999090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2931900090

[ Summary ]:
2931900090. other organo-inorganic compounds. VAT:17.0%. Tax rebate rate:13.0%. Supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward). MFN tariff:6.5%. General tariff:30.0%

Articles

Discovery of boronic acids as novel and potent inhibitors of fatty acid amide hydrolase.

J. Med. Chem. 51 , 7057-7060, (2008)

A series of commercial phenyl-, heteroaryl-, alkyl-, and alkenylboronic acids were evaluated for their FAAH and MGL inhibitory activities. The compounds were generally selective for FAAH, with IC50 in...

Related Compounds

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