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POTASSIUM PHENYLTRIFLUOROBORATE

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POTASSIUM PHENYLTRIFLUOROBORATE Basic information

Product Name:
POTASSIUM PHENYLTRIFLUOROBORATE
Synonyms:
  • Benzenetrifluoroboric acid potassium salt~Phenyltrifluoroboric acid potassium salt
  • Potassium phenylfluoroborate
  • Potassium Thienylfluoroborate
  • benzenetrifluoroboric acid potassium salt
  • phenyltrifluoroboric acid potassium salt
  • POTASSIUM PHENYLTRIFLUOROBORATE
  • potassium trifluoro(phenyl)boranuide
  • Potassium phenyltrifluoroborate,95%
CAS:
153766-81-5
MF:
C6H5BF3K
MW:
184.01
EINECS:
627-190-3
Product Categories:
  • Boronic Acids and Derivatives
  • Trifluoroborate Salts
  • blocks
  • B (Classes of Boron Compounds)
  • B-Bromocatecholborane, etc.
  • Aryl
  • Trifluoroborates
  • Boron, Nitrile, Thio,& TM-Cpds
Mol File:
153766-81-5.mol
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POTASSIUM PHENYLTRIFLUOROBORATE Chemical Properties

Melting point:
300°C
storage temp. 
Inert atmosphere,Room Temperature
form 
Powder
color 
White
Water Solubility 
Soluble in water.
BRN 
7782070
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
Hazard Note 
Irritant
HS Code 
29319090

MSDS

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POTASSIUM PHENYLTRIFLUOROBORATE Usage And Synthesis

Chemical Properties

White powder

Uses

Aryltrifluoroborate salts are more nucleophilic than the corresponding arylboronic acids and undergo ligand-free Pd-catalyzed cross-coupling reactions with arenediazonium tetrafluoroborates to give good yields of biaryls. Suzuki Cross-Coupling are conducted using organotrifluoroborates as a potent boronic acid surrogates. In the presence of Dicarbonyl-(2,4-pentanedionato)-rhodium(I)-, 39295, K aryl- and alkenyltrifluoroborates add to aldehydes and enones to give secondary alcohols and saturated ketones, respectively.

POTASSIUM PHENYLTRIFLUOROBORATESupplier

J & K SCIENTIFIC LTD.
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