4-Trifluoromethylphenylboronic acid
Names
[ CAS No. ]:
128796-39-4
[ Name ]:
4-Trifluoromethylphenylboronic acid
[Synonym ]:
QBQR DXFFF
MFCD00151855
4-(Trifluoromethyl)phenylboronic acid
Boronic acid, B-[4-(trifluoromethyl)phenyl]-
α,α,α-Trifluoro-p-tolueneboronic Acid,contains varying amounts of An
α,α,α-Trifluoro-p-tolueneboronic Acid
Dihydroxy[4-(trifluoromethyl)phenyl]borane
α,α,α-Trifluoro-p-tolylboronic acid
(4-(Trifluoromethyl)phenyl)boronic acid
4-(Trifluoromethyl)benzeneboronic acid
[4-(Trifluoromethyl)phenyl]boranediol
B-[4-(Trifluoromethyl)phenyl]boronic acid
[4-(Trifluoromethyl)phenyl]boronic acid
(4-Trifluoromethylphenyl)boronic acid
Biological Activity
[Description]:
[Related Catalog]:
[In Vitro]
Chemical & Physical Properties
[ Density]:
1.4±0.1 g/cm3
[ Boiling Point ]:
258.6±50.0 °C at 760 mmHg
[ Melting Point ]:
245-250 °C(lit.)
[ Molecular Formula ]:
C7H6BF3O2
[ Molecular Weight ]:
189.93
[ Flash Point ]:
110.2±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
Safety Information
[ Symbol ]:
GHS07
[ Signal Word ]:
Warning
[ Hazard Statements ]:
H302
[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves
[ Hazard Codes ]:
Xi:Irritant
[ Risk Phrases ]:
R36/37/38
[ Safety Phrases ]:
S37/39-S26
[ RIDADR ]:
NONH for all modes of transport
[ WGK Germany ]:
3
[ HS Code ]:
2931900090
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
Org. Lett. 7th ed., 14 , 1930-1933, (2012)
A Ru-catalyzed direct arylation of benzylic sp(3) carbons of acyclic amines with arylboronates is reported. This highly regioselective and efficient transformation can be performed with various combin...
Tandem-type Pd(II)-catalyzed oxidative Heck reaction/intramolecular C-H amidation sequence: a novel route to 4-aryl-2-quinolinones.Chem. Commun. (Camb.) 36th ed., 48 , 4332-4334, (2012)
A novel catalytic method for synthesizing 4-aryl-2-quinolinones is reported. The process involves two mechanistically independent, sequential Pd(II)-catalyzed reactions--the oxidative Heck reaction an...
Combined experimental-theoretical NMR study on 2,5-bis(5-aryl-3-hexylthiophen-2-yl)-thiazolo[5,4-d]thiazole derivatives for printable electronics.Magn. Reson. Chem. 5th ed., 50 , 379-387, (2012)
Four 2,5-bis(5-aryl-3-hexylthiophen-2-yl)thiazolo[5,4-d]thiazole derivatives have been synthesized and thoroughly characterized. The extended aromatic core of the molecules was designed to enhance the...