Atomfair Potassium trifluoro(neopentyl)borate C5H11BF3K CAS 1150655-02-9

Potassium Trifluoro(neopentyl)borate (CAS: 1150655-02-9) is a highly specialized organoboron compound with the molecular formula C5H11BF3K . This potassium salt of trifluoro(neopentyl)borate is a versatile reagent widely used in synthetic chemistry, particularly in cross-coupling reactions, due to its stability and reactivity. The neopentyl (2,2-dimethylpropyl) group enhances steric hindrance, making it valuable for selective transformations in organic synthesis. This high-purity compound is ideal for researchers and scientists working on polymer chemistry, pharmaceutical intermediates, and advanced material science . It is supplied as a white to off-white crystalline powder with stringent quality control to ensure consistency in performance. Store in a cool, dry…

Description

Potassium Trifluoro(neopentyl)borate (CAS: 1150655-02-9) is a highly specialized organoboron compound with the molecular formula C5H11BF3K. This potassium salt of trifluoro(neopentyl)borate is a versatile reagent widely used in synthetic chemistry, particularly in cross-coupling reactions, due to its stability and reactivity. The neopentyl (2,2-dimethylpropyl) group enhances steric hindrance, making it valuable for selective transformations in organic synthesis.

This high-purity compound is ideal for researchers and scientists working on polymer chemistry, pharmaceutical intermediates, and advanced material science. It is supplied as a white to off-white crystalline powder with stringent quality control to ensure consistency in performance. Store in a cool, dry place under inert conditions to maintain stability.

Key Features:

  • High reactivity in Suzuki-Miyaura and other palladium-catalyzed cross-coupling reactions
  • Excellent solubility in polar aprotic solvents (e.g., DMF, DMSO)
  • Stable under inert atmospheres with minimal decomposition
  • Strictly controlled moisture levels (<1%) for optimal performance

Properties

  • CAS Number: 1150655-02-9
  • Complexity: 94
  • IUPAC Name: potassium;2,2-dimethylpropyl(trifluoro)boranuide
  • InChI: InChI=1S/C5H11BF3.K/c1-5(2,3)4-6(7,8)9;/h4H2,1-3H3;/q-1;+1
  • InChI Key: QPXOGXAOXXGHLX-UHFFFAOYSA-N
  • Exact Mass: 178.0542965
  • Molecular Formula: C5H11BF3K
  • Molecular Weight: 178.05
  • SMILES: [B-](CC(C)(C)C)(F)(F)F.[K+]
  • Monoisotopic Mass: 178.0542965
  • Synonyms: 1150655-02-9, Potassium trifluoro(neopentyl)borate, potassium;2,2-dimethylpropyl(trifluoro)boranuide, Potassium neopentyltrifluoroborate, Borate(1-), (2,2-dimethylpropyl)trifluoro-, potassium (1:1), (T-4)-, POTASSIUM (2,2-DIMETHYLPROPYL)TRIFLUOROBORANUIDE, MFCD09271780, 2,2-DIMETHYLPROPYL TRIFLUOROBORATE POTASSIUM SALT, POTASSIUM 2,2-DIMETHYLPROPYLTRIFLUOROBORATE, DTXSID70674898, Potassiumtrifluoro(neopentyl)borate, AWB65502, AKOS016004324, AB50557, AC-33873, AS-72183, SY068095, 2,2-Dimethylpropyltrifluoroborate potassium, CS-0139546, EN300-261417, N12176, Potassium(2,2-dimethylprop-1-yl)trifluoroborate, Potassium (2,2-dimethylpropyl)(trifluoro)borate(1-), 2,2-DIMETHYLPROPYLTRIFLUOROBORATE POTASSIUM SALT

Potassium trifluoro(neopentyl)borate is primarily used as a boron nucleophile in transition metal-catalyzed cross-coupling reactions, enabling the synthesis of complex organic molecules. Its sterically hindered structure improves selectivity in C-C bond formation, making it valuable for pharmaceutical and agrochemical research. The compound is also employed in polymer modification and as a precursor for advanced boron-containing materials.

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Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.

Disclaimer

Intended Use & Restrictions

This product is sold exclusively for laboratory research, analytical testing, or non-commercial purposes.

  • Strictly prohibited: Resale, repackaging, or formulation into commercial products.
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