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Potassium trans-beta-styryltrifluoroborate, 98%, Thermo Scientific Chemicals
$112.63 - $335.82
Chemical Identifiers
CAS | 201852-49-5 |
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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 |
Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
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Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
AAL1797103
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Thermo Scientific Chemicals
L1797103 |
1 g |
Each for $112.63
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AAL1797106
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Thermo Scientific Chemicals
L1797106 |
5 g |
Each for $335.82
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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.
ApplicationsPotassium 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.
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
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
RUO – Research Use Only