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CAS 372963-48-9

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(4-methylpyridin-2-yl)boronic acid

Description:
(4-Methylpyridin-2-yl)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 pyridine ring substituted with a methyl group at the 4-position and a boronic acid group at the 2-position. It is typically a white to off-white solid that is soluble in polar solvents such as water and alcohols, owing to the presence of the boronic acid group, which can form hydrogen bonds. The compound is known for its utility in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a boron source for the formation of carbon-carbon bonds. Additionally, (4-methylpyridin-2-yl)boronic acid can participate in various coordination chemistry applications due to the ability of boron to form complexes with Lewis bases. Its reactivity and functional properties make it valuable in medicinal chemistry and materials science. Safety data should be consulted for handling and storage, as with all chemical substances.
Formula:C6H8BNO2
InChI:InChI=1/C6H8BNO2/c1-5-2-3-8-6(4-5)7(9)10/h2-4,9-10H,1H3
SMILES:Cc1ccnc(c1)B(O)O
Synonyms:
  • boronic acid, B-(4-methyl-2-pyridinyl)-
  • (4-Methylpyridin-2-yl)boronic acid
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