Atomfair Trifluoro(piperidin-1-ylmethyl)boranuide C6H12BF3N-

Description Trifluoro(piperidin-1-ylmethyl)boranuide (CAS No. 1268340-93-7) is a highly specialized organoboron compound with the molecular formula C6H12BF3N-. This anionic boron complex features a piperidine-substituted methyl group and three fluorine atoms, making it a valuable reagent for advanced synthetic and catalytic applications. Its unique structure offers exceptional reactivity in boron-mediated transformations, including cross-coupling reactions and as a precursor for boron-containing ionic liquids. With high purity and stability, this compound is ideal for researchers in organometallic chemistry, materials science, and pharmaceutical development. Proper handling under inert conditions is recommended due to its moisture-sensitive nature.

Description

Trifluoro(piperidin-1-ylmethyl)boranuide (CAS No. 1268340-93-7) is a highly specialized organoboron compound with the molecular formula C₆H₁₂BF₃N^–. This anionic boron complex features a piperidine-substituted methyl group and three fluorine atoms, making it a valuable reagent for advanced synthetic and catalytic applications. Its unique structure offers exceptional reactivity in boron-mediated transformations, including cross-coupling reactions and as a precursor for boron-containing ionic liquids. With high purity and stability, this compound is ideal for researchers in organometallic chemistry, materials science, and pharmaceutical development. Proper handling under inert conditions is recommended due to its moisture-sensitive nature.

CAS No: 1268340-93-7
Molecular Formula: C6H12BF3N-
Molecular Weight: 165.97
Exact Mass: 166.1014890
Monoisotopic Mass: 166.1014890
Charge: -1
IUPAC Name: trifluoro(piperidin-1-ylmethyl)boranuide
SMILES: [B-](CN1CCCCC1)(F)(F)F
Synonyms: SCHEMBL9959141, trifluoro(piperidin-1-ylmethyl)boranuide

Application

Trifluoro(piperidin-1-ylmethyl)boranuide serves as a versatile intermediate in organoboron chemistry, particularly in Suzuki-Miyaura cross-coupling reactions. Its anionic character enhances solubility in polar solvents, facilitating use in catalytic systems. Researchers also employ it to synthesize boron-doped organic frameworks for optoelectronic materials. Potential applications extend to anion-responsive molecular switches due to its fluorine-rich structure.

If you are interested or have any questions, please contact us at support@atomfair.com