Atomfair Trifluoro(pyridine)boron C5H5BF3N

Description Trifluoro(pyridine)boron (CAS No. 407-76-1) is a highly specialized organoboron compound with the molecular formula C5H5BF3N . This reagent is widely utilized in advanced organic synthesis, catalysis, and materials science due to its unique Lewis acidic properties. The compound features a boron center coordinated to three fluorine atoms and a pyridine ligand, making it an effective catalyst in fluorination and coupling reactions. With a purity grade suitable for research and industrial applications, it is supplied in rigorously controlled conditions to ensure stability and performance. Ideal for chemists working on novel boron-based reagents, this product is a valuable addition to any…

Description

Trifluoro(pyridine)boron (CAS No. 407-76-1) is a highly specialized organoboron compound with the molecular formula C₅H₅BF₃N. This reagent is widely utilized in advanced organic synthesis, catalysis, and materials science due to its unique Lewis acidic properties. The compound features a boron center coordinated to three fluorine atoms and a pyridine ligand, making it an effective catalyst in fluorination and coupling reactions. With a purity grade suitable for research and industrial applications, it is supplied in rigorously controlled conditions to ensure stability and performance. Ideal for chemists working on novel boron-based reagents, this product is a valuable addition to any laboratory focusing on organometallic chemistry or fluorinated compounds.

CAS No: 407-76-1
Molecular Formula: C5H5BF3N
Molecular Weight: 146.91
Exact Mass: 147.0467138
Monoisotopic Mass: 147.0467138
IUPAC Name: trifluoro(pyridin-1-ium-1-yl)boranuide
SMILES: [B-]([N+]1=CC=CC=C1)(F)(F)F
Synonyms: Trifluoro(pyridine)boron, 407-76-1, 821-070-6, trifluoro(pyridin-1-ium-1-yl)boranuide, MFCD00971931

Application

Trifluoro(pyridine)boron is primarily used as a Lewis acid catalyst in organic synthesis, particularly in fluorination and cross-coupling reactions. It serves as a key intermediate in the preparation of boron-containing polymers and advanced materials. Researchers also employ it in the development of pharmaceuticals and agrochemicals due to its ability to facilitate selective transformations. Its stability and reactivity make it suitable for use in both academic and industrial settings.

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