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CAS 930303-26-7

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(3-methylpyridin-2-yl)boronic acid

Description:
(3-Methylpyridin-2-yl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a pyridine ring. The molecular structure features a pyridine ring substituted with a methyl group at the 3-position and a boronic acid group at the 2-position. This compound is typically a white to off-white solid and 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. It exhibits properties that make it useful in organic synthesis, particularly in Suzuki coupling reactions, where it acts as a nucleophile to form carbon-carbon bonds. Additionally, (3-methylpyridin-2-yl)boronic acid can participate in complexation with diols, making it valuable in the development of sensors and in medicinal chemistry for drug design. Its reactivity and functional versatility are enhanced by the presence of both the aromatic pyridine and the boronic acid moiety, allowing for a range of applications in chemical research and industry.
Formula:C6H8BNO2
InChI:InChI=1/C6H8BNO2/c1-5-3-2-4-8-6(5)7(9)10/h2-4,9-10H,1H3
SMILES:Cc1cccnc1B(O)O
Synonyms:
  • 3-Methyl-2-pyridineboronic acid
  • boronic acid, B-(3-methyl-2-pyridinyl)-
  • (3-Methylpyridin-2-yl)boronic acid
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