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CAS 1105663-76-0

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

Description:
2-(2,4-Difluorophenoxy)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is a chemical compound characterized by its complex structure, which includes a pyridine ring substituted with a difluorophenoxy group and a boron-containing moiety. The presence of the difluorophenoxy group suggests potential applications in pharmaceuticals or agrochemicals, as fluorinated compounds often exhibit enhanced biological activity and stability. The boron-containing dioxaborolane unit may facilitate various chemical reactions, including Suzuki coupling, making it valuable in organic synthesis. This compound is likely to be a solid at room temperature, with moderate solubility in organic solvents, reflecting its polar and non-polar characteristics due to the diverse functional groups. Its molecular structure indicates potential for interactions with biological targets, and it may exhibit unique electronic properties due to the presence of fluorine and boron. Safety and handling precautions should be observed, as with any chemical, particularly those with complex functional groups. Further studies would be necessary to fully elucidate its properties and potential applications.
Formula:C17H18BF2NO3
InChI:InChI=1S/C17H18BF2NO3/c1-16(2)17(3,4)24-18(23-16)11-5-8-15(21-10-11)22-14-7-6-12(19)9-13(14)20/h5-10H,1-4H3
InChI key:InChIKey=XZPOHTCLAPXBLV-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C=2C=CC(OC3=C(F)C=C(F)C=C3)=NC2
Synonyms:
  • Pyridine, 2-(2,4-difluorophenoxy)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
  • 2-(2,4-Difluorophenoxy)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
  • 6-(2-Fluorophenoxy)pyridine-3-boronic acid
  • (6-(2-Fluorophenoxy)pyridin-3-yl)boronic acid
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