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CAS 536693-95-5

:

(2-chloro-6-methylpyridin-3-yl)boronic acid

Description:
(2-Chloro-6-methylpyridin-3-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 chlorine atom and a methyl group at specific positions on the pyridine ring, which influences its reactivity and solubility. Typically, boronic acids are known for their ability to form reversible complexes with diols, making them valuable in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. The presence of the chlorine substituent can enhance the electrophilicity of the pyridine ring, while the methyl group may affect steric hindrance and electronic properties. This compound is likely to be a solid at room temperature and may exhibit moderate solubility in polar solvents. Its applications may extend to medicinal chemistry, agrochemicals, and materials science, where boronic acids play a crucial role in the development of various chemical processes and products.
Formula:C6H7BClNO2
InChI:InChI=1/C6H7BClNO2/c1-4-2-3-5(7(10)11)6(8)9-4/h2-3,10-11H,1H3
SMILES:Cc1ccc(c(Cl)n1)B(O)O
Synonyms:
  • 2-Chloro-6-methyl-3-pyridineboronic acid
  • 2-Chloro-6-Methylpyridine-3-Boronic Acid
  • B-(2-Chloro-6-methyl-3-pyridinyl)boronic acid
  • Boronic acid, B-(2-chloro-6-methyl-3-pyridinyl)-
  • T6Nj Bg Cbqq F1 [Wln]
  • (2-Chloro-6-methylpyridin-3-yl)boronic acid
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