4-Cyanophenylboronic acid
Names
[ CAS No. ]:
126747-14-6
[ Name ]:
4-Cyanophenylboronic acid
[Synonym ]:
4-Cyanophenylboronic acid
MFCD01318968
4-Cyanobenzeneboronic Acid
Boronic acid, B-(4-cyanophenyl)-
(p-Cyanophenyl)boronic acid 4-Cyanobenzeneboronic acid 4-Cyanophenylboric acid
(4-Cyanophenyl)boronic acid
Biological Activity
[Description]:
[Related Catalog]:
Chemical & Physical Properties
[ Density]:
1.3±0.1 g/cm3
[ Boiling Point ]:
355.9±44.0 °C at 760 mmHg
[ Melting Point ]:
>350 °C(lit.)
[ Molecular Formula ]:
C7H6BNO2
[ Molecular Weight ]:
146.94
[ Flash Point ]:
169.0±28.4 °C
[ Exact Mass ]:
147.049164
[ PSA ]:
64.25000
[ LogP ]:
1.03
[ Vapour Pressure ]:
0.0±0.8 mmHg at 25°C
[ Index of Refraction ]:
1.560
[ Storage condition ]:
0-60°C
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-S37/39-S26
[ RIDADR ]:
UN3439
[ WGK Germany ]:
3
[ Packaging Group ]:
III
[ Hazard Class ]:
6.1
[ 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
Chem. Commun. (Camb.) 23th ed., 48 , 2912-2914, (2012)
The coupling reaction of aryl iodides with arylboronic acids to give biaryl compounds can be efficiently performed without adding a transition metal catalyst. The key to success is the use of dimethyl...
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...
3,5-Diaryl-2-aminopyridines as a novel class of orally active antimalarials demonstrating single dose cure in mice and clinical candidate potential.J. Med. Chem. 7th ed., 55 , 3479-3487, (2012)
A novel class of orally active antimalarial 3,5-diaryl-2-aminopyridines has been identified from phenotypic whole cell high-throughput screening of a commercially available SoftFocus kinase library. T...