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CAS 1334405-66-1

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B-(5-Chloro-6-methyl-3-pyridinyl)boronic acid

Description:
B-(5-Chloro-6-methyl-3-pyridinyl)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 atom and a methyl group at specific positions on the pyridine, which can influence its reactivity and solubility. Boronic acids are known for their ability to form reversible complexes with diols, making them valuable in various applications, including organic synthesis and medicinal chemistry. The presence of the chlorine and methyl substituents can enhance the compound's biological activity and selectivity in pharmaceutical applications. Additionally, this compound may exhibit properties such as moderate solubility in polar solvents and stability under standard laboratory conditions. Its unique structure allows for potential use in cross-coupling reactions, particularly in the formation of carbon-carbon bonds, which is a crucial step in the synthesis of complex organic molecules. Overall, B-(5-Chloro-6-methyl-3-pyridinyl)boronic acid is a versatile compound with significant implications in both research and industrial applications.
Formula:C6H7BClNO2
InChI:InChI=1S/C6H7BClNO2/c1-4-6(8)2-5(3-9-4)7(10)11/h2-3,10-11H,1H3
InChI key:InChIKey=FNHKINFYFJFHCC-UHFFFAOYSA-N
SMILES:B(O)(O)C=1C=C(Cl)C(C)=NC1
Synonyms:
  • B-(5-Chloro-6-methyl-3-pyridinyl)boronic acid
  • (5-Chloro-6-methylpyridin-3-yl)boronic acid
  • Boronic acid, B-(5-chloro-6-methyl-3-pyridinyl)-
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