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CAS 913836-15-4

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(6-chloro-2-methyl-3-pyridyl)boronic acid

Description:
(6-Chloro-2-methyl-3-pyridyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a pyridine ring. This compound features a chlorine substituent at the 6-position and a methyl group at the 2-position of the pyridine, contributing to its unique reactivity and properties. It is typically a white to off-white solid that is soluble in polar solvents such as water and alcohols, which is a characteristic of boronic acids due to their ability to form hydrogen bonds. The boronic acid moiety allows for participation in various chemical reactions, including Suzuki coupling, which is significant in organic synthesis for forming carbon-carbon bonds. Additionally, this compound may exhibit biological activity, making it of interest in medicinal chemistry. Its stability and reactivity can be influenced by the presence of the chlorine and methyl groups, which can affect its electronic properties and steric hindrance. Overall, (6-chloro-2-methyl-3-pyridyl)boronic acid is a versatile compound with applications in both synthetic and medicinal chemistry.
Formula:C6H7BClNO2
InChI:InChI=1/C6H7BClNO2/c1-4-5(7(10)11)2-3-6(8)9-4/h2-3,10-11H,1H3
SMILES:Cc1c(ccc(Cl)n1)B(O)O
Synonyms:
  • (6-Chloro-2-methylpyridin-3-yl)boronic acid
  • boronic acid, B-(6-chloro-2-methyl-3-pyridinyl)-
  • 6-Chloro-2-methylpyridine-3-boronic acid
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