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CAS 381248-04-0

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2-Chloropyridine-3-boronicacid

Description:
2-Chloropyridine-3-boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a chlorinated pyridine ring. This compound typically exhibits a white to off-white crystalline appearance and is soluble in polar solvents such as water and alcohols, owing to the boronic acid moiety. The presence of the chlorine atom on the pyridine ring influences its reactivity, making it useful in various chemical reactions, particularly in Suzuki coupling reactions, which are pivotal in the synthesis of biaryl compounds. The boronic acid group allows for the formation of stable complexes with diols and other Lewis bases, enhancing its utility in organic synthesis and medicinal chemistry. Additionally, 2-Chloropyridine-3-boronic acid may exhibit biological activity, making it a candidate for further research in pharmaceutical applications. As with many boronic acids, it is important to handle this compound with care, as it may be sensitive to moisture and air, which can affect its stability and reactivity.
Formula:C5H5BClNO2
InChI:InChI=1/C5H5BClNO2/c7-5-4(6(9)10)2-1-3-8-5/h1-3,9-10H
SMILES:c1cc(c(Cl)nc1)B(O)O
Synonyms:
  • Boronic acid, B-(2-chloro-3-pyridinyl)-
  • 2-Chloro-3-pyridylboronic acid
  • (2-Chloropyridin-3-Yl)Boronic Acid
  • 3-Chlorpyridine-3-boronic acid
  • 2-Chloro-5-Trimethoxyphenylboronic acid
  • 2-Chloropyridine-3-boronic acid
  • 2-Chloropyridin-3-Ylboronic Acid
  • AKOS BRN-0504
  • Boronic acid, (2-chloro-3-pyridinyl)-(9CI)
  • 2-Chloropyridine-3-Boronic
  • See more synonyms
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