4-Cyanophenylboronic acid

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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

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

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-S37/39-S26

[ RIDADR ]:
UN3439

[ WGK Germany ]:
3

[ Packaging Group ]:
III

[ Hazard Class ]:
6.1

[ HS Code ]:
2931900090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • 4-Cyanophenyl trifluoromethanesulfonate
  • (4-Chlorophenyl)boronic acid
  • zinc,dicyanide
  • 4-Formylphenylboronic acid
  • Potassium (4-cyanophenyl)(trifluoro)borate(1-)
  • di-isopropyl 4-cyanophenylboronate
  • 4-Chlorobenzonitrile
  • (4-cyanophenyl)trifluoroborate

DownStream

  • 4-(4-methylphenyl)sulfanylbenzonitrile
  • 4-(PYRIDIN-2-YL)BENZONITRILE
  • 4-(Trifluoromethylthio)benzonitrile
  • 4'-Methyl-4-biphenylcarbonitrile
  • 4-Amino-4'-cyanobiphenyl
  • 4-Cyanobiphenyl
  • 4,4'-Dicyanobiphenyl
  • 4-CYANO-4'-NITRODIPHENYL
  • 4-(Trifluoromethyl)benzonitrile
  • 3-Fluorobenzonitrile

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

Use of dimethyl carbonate as a solvent greatly enhances the biaryl coupling of aryl iodides and organoboron reagents without adding any transition metal catalysts.

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...


More Articles

Related Compounds

  • 2-Methyl-4-cyanophenylboronic acid
  • 2-Chloro-4-cyanophenylboronic Acid
  • 3-Chloro-4-cyanophenylboronic acid
  • 2-Amino-4-cyanophenylboronic acid,HCl
  • 4-Cyanophenylboronic acid,neopentyl glycol ester
  • 2,6-Dimethyl-4-cyanophenylboronic acid pinacol ester
  • Ethyl 5-amino-2-(phenylsulfanyl)benzoate
  • 4-Bromo-2-chloro-6-(1,1-dimethylethyl)-N-methylbenzenamine
  • 5-Methyl-2-(2,2,2-trifluoroethoxy)-benzylamine
  • (S)-N-(2-(4-((4-(Benzo[d]isothiazol-4-yloxy)-3-chlorophenyl)amino)-5H-pyrrolo[3,2-d]pyrimidin-5-yl)ethyl)pyrrolidine-2-carboxamide
  • 5-Isobutyl-4-methyl-pyridine-2-carboxylic acid isopropyl ester
  • 6-bromo-N-(2,3-dihydro-1-benzofuran-3-yl)quinolin-2-amine
  • 5-Methyl-3-phenyl-isothiazole-4-carboxylic acid ethyl ester
  • (5-Chloro-2-methylphenyl)triethoxysilane
  • 2-Iodo-3-methyl-5-sulfamoylbenzoic acid
  • Ethyl 5-amino-2-(2,2,2-trifluoroethoxy)benzoate
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