| Identification | Back Directory | [Name]
POTASSIUM BETA-STYRYLTRIFLUOROBORATE | [CAS]
201852-49-5 | [Synonyms]
Potassium b-styryltrifluoroborate potassium á-styryltrifluoroborate Potassium ~-styryltrifluoroborate Potassium trifluoro(styryl)borate POTASSIUM SS-STYRYLTRIFLUOROBORATE POTASSIUM BETA-STYRYLTRIFLUOROBORATE POTASSIUM TRANS-STYRYLTRIFLUOROBORATE á-styryltrifluoroboric acid potassium salt Potassium trifluoro(E)-2-phenylethenylborate Potassium trans-^b-styryltrifluoroborate, 98% beta-Styryltrifluoroboric acid potassium salt Potassium trifluoro(E)-2-phenyl-1-ethenylborate Potassium trans-beta-styryltrifluoroborate, 98% Potassium Trifluoro[(E)-2-Phenylvinyl]Borate(1-) potassium,trifluoro-[(E)-2-phenylethenyl]boranuide POTASSIUM BETA-STYRYLTRIFLUOROBORATE ISO 9001:2015 REACH | [EINECS(EC#)]
626-332-1 | [Molecular Formula]
C8H7BF3K | [MDL Number]
MFCD02093981 | [MOL File]
201852-49-5.mol | [Molecular Weight]
210.05 |
| Chemical Properties | Back Directory | [Melting point ]
>300°C | [form ]
solid | [Water Solubility ]
Soluble in water. | [BRN ]
7782992 | [InChI]
1S/C8H7BF3.K/c10-9(11,12)7-6-8-4-2-1-3-5-8;/h1-7H;/q-1;+1/b7-6+; | [InChIKey]
NONAUTDEFRJJII-UHDJGPCESA-N | [SMILES]
[K+].F[B-](F)(F)\C=C\c1ccccc1 |
| Hazard Information | Back Directory | [Uses]
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. | [Uses]
Reactant for:
- Suzuki-Miyaura cross-coupling
- Enantioselective total synthesis of naseseazines A and B via regioselective Friedel-Crafts based arylative dimerization
- Metal-free chlorodeboronation reactions
- Preparation of aryl ketones via Lewis acid-catalyzed nucleophilic substitution
- Preparation of Weinreb amides by palladium-catalyzed cross-coupling reactions
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Sigma-Aldrich
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