Description

Potassium (Morpholin-4-yl)methyltrifluoroborate (CAS: 936329-94-1) is a highly specialized organoboron compound with the molecular formula C₅H₁₀BF₃KNO. This reagent is widely utilized in advanced organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, due to its stability and reactivity under mild conditions. The morpholine moiety enhances solubility and compatibility with polar solvents, making it ideal for pharmaceutical and agrochemical research. Supplied as a crystalline solid with high purity (>95%), it is rigorously tested for consistency and performance in metal-catalyzed transformations. Store under inert conditions to maintain stability and avoid moisture exposure.

Properties

• CAS Number: 936329-94-1
• Complexity: 128
• IUPAC Name: potassium;trifluoro(morpholinomethyl)boranuide
• InChI: InChI=1S/C5H10BF3NO.K/c7-6(8,9)5-10-1-3-11-4-2-10;/h1-5H2;/q-1;+1
• InChI Key: KYDJCUCIKMUKQU-UHFFFAOYSA-N
• Exact Mass: 207.0444601
• Molecular Formula: C5H10BF3KNO
• Molecular Weight: 207.05
• SMILES: [B-](CN1CCOCC1)(F)(F)F.[K+]
• Topological: 12.5
• Monoisotopic Mass: 207.0444601
• Synonyms: 936329-94-1, POTASSIUM (MORPHOLIN-4-YL)METHYLTRIFLUOROBORATE, Potassium trifluoro(morpholinomethyl)borate, MFCD10566512, potassium;trifluoro(morpholin-4-ylmethyl)boranuide, Potassium (Morpholinomethyl)trifluoroborate, potassium trifluoro[(morpholin-4-yl)methyl]boranuide, SCHEMBL1026947, DTXSID40670569, KYDJCUCIKMUKQU-UHFFFAOYSA-N, AKOS005256975, AKOS015852629, CS-W003946, AC-33926, AS-65685, BP-10941, SY032279, DB-079634, potassium trifluoro(morpholinomethyl)boranuide, I12316, EN300-6475378, Potassium (morpholin-4-yl)methyl trifluoroborate, A1-24355, Potassium trifluoro[(morpholin-4-yl)methyl]borate(1-)

Potassium (Morpholin-4-yl)methyltrifluoroborate is a key intermediate in the synthesis of complex bioactive molecules, particularly in medicinal chemistry for drug discovery. It serves as a stable boronate ester precursor in palladium-catalyzed cross-coupling reactions, enabling efficient C-C bond formation. Applications extend to material science for designing boron-containing polymers. Its compatibility with aqueous systems makes it suitable for green chemistry initiatives.

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