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CAS 1150561-78-6

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3-BROMO-2-FLUOROPYRIDINE-4-BORONIC ACID PINACOL ESTER

Description:
3-Bromo-2-fluoropyridine-4-boronic acid pinacol ester is an organoboron compound characterized by the presence of a boronic acid moiety, which is typically used in Suzuki coupling reactions for the formation of carbon-carbon bonds. This compound features a pyridine ring substituted with a bromine atom and a fluorine atom, contributing to its unique reactivity and potential applications in medicinal chemistry and material science. The pinacol ester formation enhances the stability of the boronic acid, making it more suitable for various synthetic applications. In terms of physical properties, such compounds are generally solid at room temperature and may exhibit moderate solubility in organic solvents. The presence of halogen substituents can influence the electronic properties of the molecule, affecting its reactivity and interaction with other chemical species. Overall, 3-bromo-2-fluoropyridine-4-boronic acid pinacol ester is a valuable intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals.
Formula:C11H14BBrFNO2
Synonyms:
  • 3-BROMO-2-FLUOROPYRIDINE-4-BORONIC ACID PINACOL ESTER
  • Pyridine, 3-bromo-2-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
  • 3-broMo-2-fluoro-4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)pyridine
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