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CAS 1073353-50-0

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

Description:
5-Bromo-2-fluoro-3-(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 bromine and fluorine atoms, as well as a boron-containing moiety. The presence of the bromine and fluorine substituents suggests potential reactivity and applications in various chemical reactions, particularly in the fields of medicinal chemistry and materials science. The tetramethyl-1,3,2-dioxaborolane group enhances the compound's ability to participate in cross-coupling reactions, making it valuable in synthetic organic chemistry. This compound is likely to exhibit moderate to high polarity due to the electronegative halogen atoms and the boron functionality, influencing its solubility and reactivity. Additionally, the presence of multiple functional groups may allow for further derivatization, expanding its utility in research and industrial applications. Safety data and handling precautions should be considered, as with any halogenated or boron-containing compound, due to potential toxicity and environmental impact.
Formula:C11H14BBrFNO2
InChI:InChI=1S/C11H14BBrFNO2/c1-10(2)11(3,4)17-12(16-10)8-5-7(13)6-15-9(8)14/h5-6H,1-4H3
InChI key:InChIKey=LSBZMTVRIRYRDL-UHFFFAOYSA-N
SMILES:FC1=C(B2OC(C)(C)C(C)(C)O2)C=C(Br)C=N1
Synonyms:
  • 5-Bromo-2-Fluoro-3-(4,4,5,5-Tetramethyl-[1,3,2]-Dioxaborolan-2-Yl)Pyridine
  • Pyridine, 5-bromo-2-fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
  • 5-Bromo-2-fluoropyridine-3-boronic acid,pinacol ester
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