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Potassium phenyltrifluoroborate, 98%, Thermo Scientific Chemicals

Catalog Number p-7047086
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Quantity:
1 g
5 g
This item is not returnable. View return policy
To receive the discount customers must purchase three of the same product at list price in a single order to receive 33.33% discount. There is no limit to the multiples of 3 that customers can buy. Use promo code ”21615” to get your promotional price
153766-81-5
C6H5BF3K
184.01
MFCD01318172
DVAFPKUGAUFBTJ-UHFFFAOYSA-N
potassium phenyltrifluoroborate, potassium trifluoro phenyl borate, potassium trifluoro phenyl boranuide, pubchem11425, potassiumphenyltrifluoroborate, amtb100, phenyltrifluoropotassioboron v, potassium trifluoro phenyl borate 1-, potassium ion trifluoro phenyl boranuide, potassium tris fluoranyl-phenyl-boranuide
23675248
potassium;trifluoro(phenyl)boranuide
[B-](C1=CC=CC=C1)(F)(F)F.[K+]
This item is not returnable. View return policy
To receive the discount customers must purchase three of the same product at list price in a single order to receive 33.33% discount. There is no limit to the multiples of 3 that customers can buy. Use promo code ”21615” to get your promotional price
153766-81-5
C6H5BF3K
184.01
MFCD01318172
DVAFPKUGAUFBTJ-UHFFFAOYSA-N
potassium phenyltrifluoroborate, potassium trifluoro phenyl borate, potassium trifluoro phenyl boranuide, pubchem11425, potassiumphenyltrifluoroborate, amtb100, phenyltrifluoropotassioboron v, potassium trifluoro phenyl borate 1-, potassium ion trifluoro phenyl boranuide, potassium tris fluoranyl-phenyl-boranuide
23675248
potassium;trifluoro(phenyl)boranuide
[B-](C1=CC=CC=C1)(F)(F)F.[K+]

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.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
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.

Solubility
Soluble in water.

Notes
Store in cool dry conditions in well sealed containers. Incompatible with strong oxidizing agents.
TRUSTED_SUSTAINABILITY
Melting Point 296°C to 301°C
Quantity 1 g
Beilstein 7782070
Solubility Information Soluble in water.
Formula Weight 184
Percent Purity 98%
Chemical Name or Material Potassium phenyltrifluoroborate

RUO – Research Use Only

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