| Identification | Back Directory | [Name]
POTASSIUM PHENYLTRIFLUOROBORATE | [CAS]
153766-81-5 | [Synonyms]
Potassium phenylfluoroborate
Potassium Thienylfluoroborate
POTASSIUM PHENYLTRIFLUOROBORATE
potassiuM trifluoro(phenyl)borate
Potassium phenyltrifluoroborate 98%
Potassium phenyltrifluoroborate,95%
phenyltrifluoroboric acid potassium salt
benzenetrifluoroboric acid potassium salt
Benzenetrifluoroboric acid potassium salt~Phenyltrifluoroboric acid potassium salt | [EINECS(EC#)]
-0 | [Molecular Formula]
C6H5BF3K | [MDL Number]
MFCD01318172 | [MOL File]
153766-81-5.mol | [Molecular Weight]
184.01 |
| Chemical Properties | Back Directory | [Appearance]
White powder | [Melting point ]
300°C | [storage temp. ]
Inert atmosphere,Room Temperature | [form ]
Powder | [color ]
White | [Water Solubility ]
Soluble in water. | [BRN ]
7782070 |
| Hazard Information | Back Directory | [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. |
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