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CAS 1072945-00-6

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2,6-difluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine

Description:
2,6-Difluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is a chemical compound characterized by its unique structure, which includes a pyridine ring substituted with two fluorine atoms at the 2 and 6 positions and a boron-containing moiety at the 3 position. The presence of the dioxaborolane group enhances its reactivity and solubility in various organic solvents, making it useful in synthetic chemistry, particularly in cross-coupling reactions. This compound is typically stable under standard laboratory conditions but may undergo hydrolysis in the presence of moisture due to the boron atom's affinity for water. Its fluorinated nature can impart unique electronic properties, potentially influencing its behavior in biological systems or materials science applications. Additionally, the compound's structure suggests potential applications in medicinal chemistry, where fluorinated compounds often exhibit improved pharmacokinetic properties. Overall, 2,6-difluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is a versatile building block in organic synthesis and materials development.
Formula:C11H14BF2NO2
InChI:InChI=1/C11H14BF2NO2/c1-10(2)11(3,4)17-12(16-10)7-5-6-8(13)15-9(7)14/h5-6H,1-4H3
SMILES:CC1(C)C(C)(C)OB(c2ccc(F)nc2F)O1
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