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CAS 652148-97-5

:

(5-bromopyridin-2-yl)boronic acid

Description:
(5-Bromopyridin-2-yl)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 a bromine atom. This compound typically exhibits a white to off-white crystalline appearance and is soluble in polar solvents such as water and alcohols, which is a common trait of boronic acids due to their ability to form hydrogen bonds. The presence of the bromine atom enhances its reactivity, making it useful in various chemical reactions, including Suzuki coupling, which is a method for forming carbon-carbon bonds. Additionally, the boronic acid group allows for the formation of stable complexes with diols, making it valuable in medicinal chemistry and materials science. Its unique structural features contribute to its applications in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. As with many boronic acids, it is important to handle this compound with care, as it may have specific safety and environmental considerations.
Formula:C5H5BBrNO2
InChI:InChI=1/C5H5BBrNO2/c7-4-1-2-5(6(9)10)8-3-4/h1-3,9-10H
Synonyms:
  • boronic acid, B-(5-bromo-2-pyridinyl)-
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