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CAS 693774-55-9

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(2,6-dimethylpyridin-3-yl)boronic acid

Description:
(2,6-Dimethylpyridin-3-yl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a pyridine ring that has two methyl substituents at the 2 and 6 positions and a boron atom bonded to a hydroxyl group. This compound typically exhibits properties such as moderate solubility in polar organic solvents and water, making it useful in various chemical reactions, particularly in Suzuki coupling reactions, which are essential for forming carbon-carbon bonds in organic synthesis. The presence of the boronic acid group allows for the formation of stable complexes with diols, enhancing its utility in medicinal chemistry and materials science. Additionally, the methyl groups on the pyridine ring can influence the electronic properties and steric hindrance, affecting reactivity and selectivity in chemical reactions. Overall, (2,6-dimethylpyridin-3-yl)boronic acid is a valuable compound in synthetic organic chemistry, particularly in the development of pharmaceuticals and agrochemicals.
Formula:C7H10BNO2
InChI:InChI=1/C7H10BNO2/c1-5-3-4-7(8(10)11)6(2)9-5/h3-4,10-11H,1-2H3
SMILES:Cc1ccc(c(C)n1)B(O)O
Synonyms:
  • 2,6-Dimethylpyridine-3-boronic acid
  • boronic acid, B-(2,6-dimethyl-3-pyridinyl)-
  • 2,6-Domethylpyridine-3-boronic acid
  • (2,6-Dimethylpyridin-3-yl)boronic acid
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