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CAS 458532-86-0

:

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

Description:
2-Fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is an organic compound characterized by its unique structure, which includes a pyridine ring substituted with a fluorine atom and a boron-containing moiety. The presence of the fluorine atom enhances its reactivity and potential applications in various chemical reactions, particularly in medicinal chemistry and materials science. The dioxaborolane group contributes to its stability and solubility in organic solvents, making it useful in synthetic pathways, especially in cross-coupling reactions. This compound may exhibit interesting electronic properties due to the electron-withdrawing nature of the fluorine atom and the electron-donating characteristics of the boron moiety. Additionally, its structural features suggest potential applications in the development of pharmaceuticals or agrochemicals, where selective reactivity is crucial. Overall, 2-Fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is a versatile compound with significant implications in organic synthesis and material development.
Formula:C11H15BFNO2
InChI:InChI=1S/C11H15BFNO2/c1-10(2)11(3,4)16-12(15-10)8-5-6-14-9(13)7-8/h5-7H,1-4H3
InChI key:InChIKey=PCLMNCBIXQQRMB-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C=2C=C(F)N=CC2
Synonyms:
  • 2-(2-Fluoropyridin-4-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • 2-Fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
  • 2-Fluoro-4-(tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
  • Pyridine, 2-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
  • 2-Fluoropyridine-4-boronic acid pinacol ester
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