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CAS 501435-91-2

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5-Bromo-2-fluoropyridine-3-boronic acid

Description:
5-Bromo-2-fluoropyridine-3-boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a pyridine ring that is substituted with both bromine and fluorine atoms. This compound typically appears as a solid and is soluble in polar solvents such as water and alcohols, owing to the boronic acid group, which can form hydrogen bonds. The presence of the bromine and fluorine substituents on the pyridine ring can influence its reactivity and interactions in various chemical reactions, particularly in cross-coupling reactions, where boronic acids are commonly utilized as reagents. The compound's structure allows it to participate in Suzuki-Miyaura coupling reactions, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, the unique electronic properties imparted by the halogen substituents can affect its acidity and nucleophilicity, making it a versatile building block in organic synthesis. Safety data should be consulted for handling and storage, as with all chemical substances.
Formula:C5H4BBrFNO2
InChI:InChI=1/C5H4BBrFNO2/c7-3-1-4(6(10)11)5(8)9-2-3/h1-2,10-11H
SMILES:c1c(cnc(c1B(O)O)F)Br
Synonyms:
  • 5-Bromo-2-fluoro-3-pyridylboronic acid
  • (5-Bromo-2-Fluoropyridin-3-Yl)Boronic Acid
  • 2-Fluoro-5-Bromopyridine-3-Boronic Acid
  • 5-BROMO-2-FLUOROPYRIDINE-3-BORONIC ACID
  • 5-BROMO-2-FLUOROPYRIDIE-3-BORONIC ACID
  • (5-BROMO-2-FLUORO-3-PYRIDINYL)-BORONIC ACID
  • 5-BROMO-2-FLUOROPYRIDIN-3-YLBORONIC ACID
  • 5-BROMO-2-FLUORO-3-PYRIDINEBORONIC ACID
  • 5-Bromo-2-Fluoropyridine-3-Bor
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