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Potassium trans-beta-styryltrifluoroborate, 98%, Thermo Scientific Chemicals

Catalog Number p-7047201
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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
201852-49-5
C8H7BF3K
210.05
MFCD02093981
NONAUTDEFRJJII-UHFFFAOYSA-N
potassium trans-styryltrifluoroborate, potassium beta-styryltrifluoroborate, beta-styryltrifluoroboric acid potassium salt, pubchem11312, potassiostyryltrifluoroboron v, potassium-styryltrifluoroborate, potassium a-styryltrifluoroborate, potassium b-styryltrifluoroborate, potassium e-styryltrifluoroborate, potassium 2-phenylethenyltrifluoroborate
23664278
potassium;trifluoro-[(E)-2-phenylethenyl]boranuide
[K+].F[B-](F)(F)C=CC1=CC=CC=C1
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
201852-49-5
C8H7BF3K
210.05
MFCD02093981
NONAUTDEFRJJII-UHFFFAOYSA-N
potassium trans-styryltrifluoroborate, potassium beta-styryltrifluoroborate, beta-styryltrifluoroboric acid potassium salt, pubchem11312, potassiostyryltrifluoroboron v, potassium-styryltrifluoroborate, potassium a-styryltrifluoroborate, potassium b-styryltrifluoroborate, potassium e-styryltrifluoroborate, potassium 2-phenylethenyltrifluoroborate
23664278
potassium;trifluoro-[(E)-2-phenylethenyl]boranuide
[K+].F[B-](F)(F)C=CC1=CC=CC=C1

Potassium trans-beta-styryltrifluoroborate is used as a reactant for Suzuki-Miyaura cross-coupling, in enantioselective total synthesis of naseseazines A and B via regioselective Friedel-Crafts based arylative dimerization, in metal-free chlorodeboronation reactions, in preparation of aryl ketones via Lewis acid-catalyzed nucleophilic substitution and in preparation of Weinreb amides by palladium-catalyzed cross-coupling reactions.

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
Potassium trans-beta-styryltrifluoroborate is used as a reactant for Suzuki-Miyaura cross-coupling, in enantioselective total synthesis of naseseazines A and B via regioselective Friedel-Crafts based arylative dimerization, in metal-free chlorodeboronation reactions, in preparation of aryl ketones via Lewis acid-catalyzed nucleophilic substitution and in preparation of Weinreb amides by palladium-catalyzed cross-coupling reactions.

Solubility
Soluble in water.

Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Incompatible with strong oxidizing agents.
TRUSTED_SUSTAINABILITY
Melting Point >300°C
Quantity 1 g
Beilstein 7782992
Solubility Information Soluble in water.
Formula Weight 210.05
Percent Purity 98%
Chemical Name or Material Potassium trans-beta-styryltrifluoroborate

RUO – Research Use Only

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