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CAS 652148-90-8

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(6-chloropyridin-2-yl)boronic acid

Description:
(6-Chloropyridin-2-yl)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 at the 6-position of the pyridine ring influences its reactivity and can enhance its utility in various chemical reactions, particularly in Suzuki coupling reactions, which are pivotal in organic synthesis for forming carbon-carbon bonds. The boronic acid group allows for the formation of reversible complexes with diols, making it useful in sensor applications and in the development of drug delivery systems. Additionally, (6-chloropyridin-2-yl)boronic acid may exhibit biological activity, making it of interest in medicinal chemistry. Its stability under standard laboratory conditions and its reactivity with various electrophiles further contribute to its significance in synthetic organic chemistry.
Formula:C5H5BClNO2
InChI:InChI=1/C5H5BClNO2/c7-5-3-1-2-4(8-5)6(9)10/h1-3,9-10H
SMILES:c1cc(B(O)O)nc(c1)Cl
Synonyms:
  • 6-Chloropyridine-2-boronicacid
  • boronic acid, B-(6-chloro-2-pyridinyl)-
  • 2-chloro-6-(dihydroxy-l3-bromanyl)pyridine
  • B-(6-Chloro-2-pyridinyl)boronic acid
  • 2-Borono-6-chloropyridine
  • (6-Chloro-2-pyridinyl)boronic acid
  • 6-chloropyridin-2-yl-2-boronic
  • (6-Chloro-2-pyridyl)boronic acid
  • (6-CHLORO-2-PYRIDINYL)BORONIC ACID; B-(6-CHLORO-2-PYRIDINYL)BORONIC ACID
  • 6-Chloro-2-pyridineboronic acid
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