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Atomfair Potassium trifluoro[(pyrrolidin-1-yl)methyl]borate C5H10BF3KN CAS 888711-53-3

Potassium Trifluoro[(pyrrolidin-1-yl)methyl]borate (CAS No. 888711-53-3) is a highly specialized organoboron compound with the molecular formula C5H10BF3KN. This advanced chemical reagent is designed for research and industrial applications, particularly in organic synthesis, catalysis, and materials science. The compound features a pyrrolidine-substituted trifluoroborate moiety, offering unique reactivity and stability for cross-coupling reactions, Suzuki-Miyaura couplings, and other boron-mediated transformations. Its high purity (>95%) ensures consistent performance in sensitive applications, while its potassium counterion enhances solubility in polar solvents. Packaged under inert conditions to prevent degradation, this reagent is ideal for pharmaceutical intermediates, agrochemical development, and advanced material design. Store in a cool, dry…

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Description

Potassium Trifluoro[(pyrrolidin-1-yl)methyl]borate (CAS No. 888711-53-3) is a highly specialized organoboron compound with the molecular formula C5H10BF3KN. This advanced chemical reagent is designed for research and industrial applications, particularly in organic synthesis, catalysis, and materials science. The compound features a pyrrolidine-substituted trifluoroborate moiety, offering unique reactivity and stability for cross-coupling reactions, Suzuki-Miyaura couplings, and other boron-mediated transformations. Its high purity (>95%) ensures consistent performance in sensitive applications, while its potassium counterion enhances solubility in polar solvents. Packaged under inert conditions to prevent degradation, this reagent is ideal for pharmaceutical intermediates, agrochemical development, and advanced material design. Store in a cool, dry place away from moisture and oxidizing agents.

Properties

  • CAS Number: 888711-53-3
  • Complexity: 113
  • IUPAC Name: potassium;trifluoro(pyrrolidin-1-ylmethyl)boranuide
  • InChI: InChI=1S/C5H10BF3N.K/c7-6(8,9)5-10-3-1-2-4-10;/h1-5H2;/q-1;+1
  • InChI Key: IPPVCGNMEPSDMN-UHFFFAOYSA-N
  • Exact Mass: 191.0495455
  • Molecular Formula: C5H10BF3KN
  • Molecular Weight: 191.05
  • SMILES: [B-](CN1CCCC1)(F)(F)F.[K+]
  • Topological: 3.2
  • Monoisotopic Mass: 191.0495455
  • Synonyms: 888711-53-3, Potassium trifluoro[(pyrrolidin-1-yl)methyl]borate, Potassium 1-trifluoroboratomethylpyrrolidine, Potassium;trifluoro(pyrrolidin-1-ylmethyl)boranuide, potassium trifluoro(pyrrolidin-1-ylmethyl)borate, Potassiumtrifluoro[(pyrrolidin-1-yl)methyl]borate, Potassium [(pyrrolidin-1-yl)methyl]trifluoroborate, Borate(1-), trifluoro(1-pyrrolidinylmethyl)-, potassium, (T-4)-, MFCD10700161, SCHEMBL15069563, DTXSID00670580, IPPVCGNMEPSDMN-UHFFFAOYSA-N, SBB091232, AKOS013014745, AC-33921, AS-68613, DB-050625, potassium 1-trifluoroboratom-ethylpyrrolidine, potassium pyrrolidin-1-ylmethyltrifluoroborate, I12230, potassium,trifluoro(pyrrolidin-1-ylmethyl)boranuide, A1-00695, potassium trifluoro[(pyrrolidin-1-yl)methyl]boranuide, Potassium trifluoro[(pyrrolidin-1-yl)methyl]borate(1-)

Potassium Trifluoro[(pyrrolidin-1-yl)methyl]borate serves as a versatile building block in organic synthesis, enabling efficient C-C bond formations via transition-metal-catalyzed reactions. It is particularly valuable in Suzuki-Miyaura cross-coupling for constructing complex heterocycles and pharmaceuticals. Researchers also utilize it in PET radiochemistry for boron-neutron capture therapy (BNCT) precursors. Its stability under aqueous conditions makes it suitable for late-stage functionalization in drug discovery.

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Disclaimer

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  • Strictly prohibited: Resale, repackaging, or formulation into commercial products.
  • Not approved for human/animal use, diagnostics, or manufacturing (including pharmaceuticals, agrochemicals, or consumer goods).

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