4-Fluorobenzeneboronic acid
Names
[ CAS No. ]:
1765-93-1
[ Name ]:
4-Fluorobenzeneboronic acid
[Synonym ]:
p-fluorophenylboronic acid
QBQR DF
4-Fluorophenylboronic Acid
p-fluorobenzeneboronic acid
(4-fluorophenyl)dihydroxyborane
(4-Fluorophenyl)boronic acid
Boronic acid, B-(4-fluorophenyl)-
MFCD00039136
4-Fluorobenzeneboronic acid
B-(4-Fluorophenyl)boronic acid
Biological Activity
[Description]:
[Related Catalog]:
Chemical & Physical Properties
[ Density]:
1.3±0.1 g/cm3
[ Boiling Point ]:
258.4±42.0 °C at 760 mmHg
[ Melting Point ]:
262-265 °C(lit.)
[ Molecular Formula ]:
C6H6BFO2
[ Molecular Weight ]:
139.92
[ Flash Point ]:
110.1±27.9 °C
[ Exact Mass ]:
140.044495
[ PSA ]:
40.46000
[ LogP ]:
1.64
[ Vapour Pressure ]:
0.0±0.6 mmHg at 25°C
[ Index of Refraction ]:
1.509
[ Storage condition ]:
0-6°C
MSDS
Safety Information
[ Symbol ]:
GHS07
[ Signal Word ]:
Warning
[ Hazard Statements ]:
H302-H315-H319-H335
[ Precautionary Statements ]:
P280-P301 + P312 + P330-P305 + P351 + P338-P337 + P313
[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves
[ 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 ]:
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. 8 , 5987, (2006)
[Structure: see text] A cationic palladium complex catalyzed addition of arylboronic acids to nitriles to yield aryl ketones with moderate to good yields was developed. A one-step synthesis of benzofu...
Ruthenium(0)-catalyzed sp3 C-H bond arylation of benzylic amines using arylboronates.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...