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CAS 1003043-40-0

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2-Chloro-3-Methylpyridine-5-Boronic Acid

Description:
2-Chloro-3-Methylpyridine-5-Boronic Acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its reactivity in various organic synthesis applications, particularly in Suzuki coupling reactions. This compound features a pyridine ring, which is a six-membered aromatic ring containing one nitrogen atom, and it is substituted with a chlorine atom and a methyl group at specific positions. The boronic acid group imparts properties that facilitate the formation of covalent bonds with diols, making it useful in the development of pharmaceuticals and agrochemicals. The presence of the chlorine atom can influence the compound's reactivity and solubility, while the methyl group can affect steric hindrance and electronic properties. Overall, 2-Chloro-3-Methylpyridine-5-Boronic Acid is a valuable intermediate in synthetic chemistry, particularly in the construction of complex molecular architectures. Its unique structural features allow for diverse applications in medicinal chemistry and materials science.
Formula:C6H7BClNO2
InChI:InChI=1/C6H7BClNO2/c1-4-2-5(7(10)11)3-9-6(4)8/h2-3,10-11H,1H3
SMILES:Cc1cc(cnc1Cl)B(O)O
Synonyms:
  • (6-Chloro-5-Methylpyridin-3-Yl)Boronic Acid
  • B-(6-Chloro-5-methyl-3-pyridinyl)boronic acid
  • Boronic acid, B-(6-chloro-5-methyl-3-pyridinyl)-
  • 6-Chloro-5-methylpyridine-3-boronic acid
  • 6-Chloro-5-methylpyridine-3-boronicacid
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