CAS 401816-16-8
:2,6-Difluoropyridine-4-boronic acid
Description:
2,6-Difluoropyridine-4-boronic acid is an organoboron compound characterized by the presence of both a pyridine ring and a boronic acid functional group. The molecular structure features a pyridine ring substituted with two fluorine atoms at the 2 and 6 positions and a boronic acid group at the 4 position. This compound is typically used in organic synthesis, particularly in Suzuki coupling reactions, which are valuable for forming carbon-carbon bonds. The presence of fluorine atoms can enhance the compound's reactivity and influence its electronic properties, making it useful in medicinal chemistry and materials science. Additionally, boronic acids are known for their ability to form reversible complexes with diols, which can be exploited in various applications, including drug delivery and sensor development. The compound is generally stable under standard conditions but may require careful handling due to its reactivity and potential environmental impact. As with many organoboron compounds, it is important to consider safety data and proper disposal methods when working with this substance.
Formula:C5H4BF2NO2
Synonyms:- 2,6-Difluoropyridin-4-ylboronic acid
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Found 3 products.
(2,6-difluoropyridin-4-yl)boronic acid
CAS:Formula:C5H4BF2NO2Purity:95%Color and Shape:SolidMolecular weight:158.89862,6-Difluoropyridine-4-boronic acid
CAS:<p>2,6-Difluoropyridine-4-boronic acid</p>Formula:C5H4BF2NO2Purity:≥95%Color and Shape: white powderMolecular weight:158.90g/mol(2,6-Difluoropyridin-4-yl)boronic acid
CAS:Formula:C5H4BF2NO2Purity:95%Color and Shape:SolidMolecular weight:158.9


