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2,6-Difluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
For research use only. Not for therapeutic Use.
2,6-Difluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is a boronic ester derivative of pyridine, featuring two fluorine atoms at the 2 and 6 positions and a boronate group at the 4 position. This compound is commonly used in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules. It is of significant interest in medicinal and materials chemistry for the creation of bioactive compounds, pharmaceuticals, and functional materials due to its versatile reactivity.
Catalog Number | M143754 |
CAS Number | 1204333-58-3 |
Molecular Formula | C11H14BF2NO2 |
Purity | ≥95% |
Storage | -20 ℃ |
IUPAC Name | 2,6-difluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine |
InChI | InChI=1S/C11H14BF2NO2/c1-10(2)11(3,4)17-12(16-10)7-5-8(13)15-9(14)6-7/h5-6H,1-4H3 |
InChIKey | FUGGRIAHIVRPNM-UHFFFAOYSA-N |
SMILES | B1(OC(C(O1)(C)C)(C)C)C2=CC(=NC(=C2)F)F |