| 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 |
| 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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