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CAS 452972-14-4

:

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

Description:
2-Fluoro-3-(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 medicinal chemistry and materials science. The dioxaborolane group contributes to its stability and solubility in various solvents, making it useful in synthetic chemistry, particularly in cross-coupling reactions. This compound is likely to exhibit moderate polarity due to the electronegative fluorine and the boron atom, which can participate in coordination chemistry. Additionally, the bulky tetramethyl substituents on the dioxaborolane enhance steric hindrance, influencing its reactivity and interactions with other molecules. Overall, this compound is of interest for its potential applications in drug development and as a building block in organic synthesis. Safety data and handling precautions should be considered, as with any chemical substance, to ensure proper laboratory practices.
Formula:C11H15BFNO2
InChI:InChI=1/C11H15BFNO2/c1-10(2)11(3,4)16-12(15-10)8-6-5-7-14-9(8)13/h5-7H,1-4H3
InChI key:InChIKey=YYOZFGQOPNTVGM-UHFFFAOYSA-N
SMILES:FC1=C(B2OC(C)(C)C(C)(C)O2)C=CC=N1
Synonyms:
  • 2-(2-Fluoro-3-pyridyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • 2-Fluoro-3-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Pyridine
  • 2-Fluoro-3-(tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
  • Pyridine, 2-Fluoro-3-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)-
  • 2-Fluoropyridine-3-boronic acid pinacol ester
  • 2-Fluoropyridine-3-boronic acid pinacol ester ,98%
  • 2-Fluoropyridine-3-boronic&nbsp
  • pyridine, 2-fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborol
  • 2-Fluoropyridine-3-boronic acid pinacol ester, 95% (H27485)
  • 2-FLUOROPYRIDINE-3-BORONIC ACID PICOL ESTER
  • See more synonyms
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