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CAS 1218790-39-6

:

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

Description:
5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2-(trifluoromethyl)pyridine is a chemical compound characterized by its unique structural features, which include a pyridine ring substituted with a trifluoromethyl group and a boron-containing dioxaborolane moiety. The presence of the trifluoromethyl group enhances its lipophilicity and can influence its reactivity and interaction with biological systems. The dioxaborolane unit contributes to the compound's potential as a versatile building block in organic synthesis, particularly in cross-coupling reactions. This compound is likely to exhibit properties typical of both pyridine derivatives and boron-containing compounds, such as moderate to high stability under standard conditions, potential reactivity in nucleophilic substitution reactions, and possible applications in medicinal chemistry and materials science. Its specific applications may depend on its reactivity profile and the ability to form complexes with various substrates. As with many boron-containing compounds, it may also exhibit interesting electronic properties due to the presence of the boron atom.
Formula:C12H15BF3NO2
InChI:InChI=1S/C12H15BF3NO2/c1-10(2)11(3,4)19-13(18-10)8-5-6-9(17-7-8)12(14,15)16/h5-7H,1-4H3
InChI key:InChIKey=SOMIPHAQTXODQM-UHFFFAOYSA-N
SMILES:CC1(C)C(C)(C)OB(c2ccc(C(F)(F)F)nc2)O1
Synonyms:
  • 2-Trifluoromethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
  • 2-Trifluoromethylpyridine-5-boronic acid pinacol ester
  • Pyridine, 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2-(trifluoromethyl)-
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