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Atomfair Potassium (cyclopentylmethyl)trifluoroboranuide C6H11BF3K

Description Potassium (cyclopentylmethyl)trifluoroboranuide (CAS No. 331282-37-2) is a highly specialized organoboron compound with the molecular formula C6H11BF3K . This potassium trifluoroborate salt is a stable, air- and moisture-resistant reagent, ideal for Suzuki-Miyaura cross-coupling reactions in organic synthesis. Its cyclopentylmethyl group enhances steric control, making it valuable for constructing complex molecular architectures. With a purity of ??95%, this compound is rigorously tested via NMR, HPLC, and elemental analysis to ensure consistency for research applications. Packaged under inert gas to preserve stability, it is suited for pharmaceutical, agrochemical, and materials science research.

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Description

Description

Potassium (cyclopentylmethyl)trifluoroboranuide (CAS No. 331282-37-2) is a highly specialized organoboron compound with the molecular formula C6H11BF3K. This potassium trifluoroborate salt is a stable, air- and moisture-resistant reagent, ideal for Suzuki-Miyaura cross-coupling reactions in organic synthesis. Its cyclopentylmethyl group enhances steric control, making it valuable for constructing complex molecular architectures. With a purity of ??95%, this compound is rigorously tested via NMR, HPLC, and elemental analysis to ensure consistency for research applications. Packaged under inert gas to preserve stability, it is suited for pharmaceutical, agrochemical, and materials science research.

  • CAS No: 331282-37-2
  • Molecular Formula: C6H11BF3K
  • Molecular Weight: 190.06
  • Exact Mass: 190.0542965
  • Monoisotopic Mass: 190.0542965
  • IUPAC Name: potassium;cyclopentylmethyl(trifluoro)boranuide
  • SMILES: [B-](CC1CCCC1)(F)(F)F.[K+]
  • Synonyms: potassium (cyclopentylmethyl)trifluoroboranuide, 968-470-8, POTASSIUM CYCLOPENTYLMETHYLTRIFLUOROBORATE, 331282-37-2, Potassium (cyclopentylmethyl)trifluoroborate

Application

Potassium (cyclopentylmethyl)trifluoroboranuide is primarily used as a coupling partner in Suzuki-Miyaura cross-coupling reactions, enabling the formation of C-C bonds in medicinal chemistry and material science. Its stability and reactivity make it ideal for synthesizing cyclopentyl-substituted compounds, which are common motifs in bioactive molecules. Researchers also employ it in the development of boron-containing polymers and catalysts.

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