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Atomfair Potassium Allyltrifluoroborate C3H5BF3K

Description Potassium Allyltrifluoroborate (CAS: 395083-14-4) is a highly versatile organoboron compound with the molecular formula C3H5BF3K . This stable, crystalline solid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, due to its excellent reactivity and handling properties. Its IUPAC name, potassium;trifluoro(prop-2-enyl)boranuide , reflects its precise chemical structure. With a purity of ??95%, this reagent is ideal for researchers and scientists seeking reliable performance in advanced synthetic applications. Each batch undergoes rigorous QC testing to ensure consistency and suitability for sensitive reactions. Available in various quantities, it is packaged under inert conditions to maintain stability.

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Description

Description

Potassium Allyltrifluoroborate (CAS: 395083-14-4) is a highly versatile organoboron compound with the molecular formula C3H5BF3K. This stable, crystalline solid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, due to its excellent reactivity and handling properties. Its IUPAC name, potassium;trifluoro(prop-2-enyl)boranuide, reflects its precise chemical structure. With a purity of ??95%, this reagent is ideal for researchers and scientists seeking reliable performance in advanced synthetic applications. Each batch undergoes rigorous QC testing to ensure consistency and suitability for sensitive reactions. Available in various quantities, it is packaged under inert conditions to maintain stability.

  • CAS No: 395083-14-4
  • Molecular Formula: C3H5BF3K
  • Molecular Weight: 147.98
  • Exact Mass: 148.0073463
  • Monoisotopic Mass: 148.0073463
  • IUPAC Name: potassium;trifluoro(prop-2-enyl)boranuide
  • SMILES: [B-](CC=C)(F)(F)F.[K+]
  • Synonyms: Potassium allyltrifluoroborate, 678-439-8, 233664-53-4, potassium;trifluoro(prop-2-enyl)boranuide, Borate(1-), trifluoro-2-propen-1-yl-, potassium, (T-4)-

Application

Potassium Allyltrifluoroborate is a key reagent in palladium-catalyzed cross-coupling reactions, enabling the introduction of allyl groups into complex organic frameworks. It is particularly valuable in pharmaceutical and agrochemical research for constructing carbon-carbon bonds. The compound’s stability in air and moisture simplifies handling compared to other boronate derivatives. Its applications extend to materials science for functionalized polymer synthesis.

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