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

$112.63 - $335.82

Chemical Identifiers

CAS 201852-49-5
Molecular Formula C8H7BF3K
Molecular Weight (g/mol) 210.05
MDL Number MFCD02093981
InChI Key NONAUTDEFRJJII-UHFFFAOYSA-N
Synonym 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
PubChem CID 23664278
IUPAC Name potassium;trifluoro-[(E)-2-phenylethenyl]boranuide
SMILES [K+].F[B-](F)(F)C=CC1=CC=CC=C1
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Products 2
Catalog Number Mfr. No. Quantity Price Quantity  
Catalog Number Mfr. No. Quantity Price Quantity  
AAL1797103
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Thermo Scientific Chemicals
L1797103
1 g
Each for $112.63
 
AAL1797106
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Thermo Scientific Chemicals
L1797106
5 g
Each for $335.82
 
Description

Description

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.
Specifications

Chemical Identifiers

201852-49-5
210.05
NONAUTDEFRJJII-UHFFFAOYSA-N
23664278
[K+].F[B-](F)(F)C=CC1=CC=CC=C1
C8H7BF3K
MFCD02093981
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
potassium;trifluoro-[(E)-2-phenylethenyl]boranuide

Specifications

201852-49-5
C8H7BF3K
1 g
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
NONAUTDEFRJJII-UHFFFAOYSA-N
potassium;trifluoro-[(E)-2-phenylethenyl]boranuide
23664278
98%
>300°C
MFCD02093981
7782992
Soluble in water.
[K+].F[B-](F)(F)C=CC1=CC=CC=C1
210.05
210.05
Potassium trans-beta-styryltrifluoroborate
Safety and Handling

Safety and Handling

GHS H Statement
H315-H319-H335
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.

P261-P264b-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P362-P501c

H315-H319-H335

EINECSNumber : 000-000-0

TSCA : No

Recommended Storage : Ambient temperatures

SDS
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RUO – Research Use Only