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CAS 1310384-07-6

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

Description:
2-Fluoro-6-methyl-4-(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 a fluorine atom and a methyl group, as well as a boron-containing moiety. The presence of the fluorine atom enhances its reactivity and potential applications in medicinal chemistry, particularly in the development of pharmaceuticals. The dioxaborolane group contributes to its stability and solubility, making it suitable for various synthetic applications, including cross-coupling reactions in organic synthesis. This compound may exhibit interesting electronic properties due to the electron-withdrawing nature of the fluorine and the electron-donating characteristics of the boron moiety. Its specific applications can vary, but it is often explored in the context of agrochemicals and advanced materials. As with many boron-containing compounds, it may also play a role in catalysis and the formation of organoboron intermediates in synthetic pathways. Safety and handling precautions should be observed due to the potential reactivity of its functional groups.
Formula:C12H17BFNO2
InChI:InChI=1S/C12H17BFNO2/c1-8-6-9(7-10(14)15-8)13-16-11(2,3)12(4,5)17-13/h6-7H,1-5H3
InChI key:InChIKey=RCTCBYOELKRFJW-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C=2C=C(C)N=C(F)C2
Synonyms:
  • Pyridine, 2-fluoro-6-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
  • 2-Fluoro-6-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
  • 2-FLUORO-6-METHYLPYRIDINE-4-BORONIC ACID PINACOL ESTER
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