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CAS 913835-86-6

:

B-(2-Chloro-5-methyl-3-pyridinyl)boronic acid

Description:
B-(2-Chloro-5-methyl-3-pyridinyl)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, which can influence its reactivity and solubility. 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 provide steric hindrance, affecting the compound's reactivity. B-(2-Chloro-5-methyl-3-pyridinyl)boronic acid is typically used in medicinal chemistry and material science, where it can serve as a building block for the synthesis of more complex molecules. Its properties, such as solubility in organic solvents and stability under various conditions, make it a useful reagent in various chemical applications.
Formula:C6H7BClNO2
InChI:InChI=1S/C6H7BClNO2/c1-4-2-5(7(10)11)6(8)9-3-4/h2-3,10-11H,1H3
InChI key:InChIKey=ZMHWEBDZKPQNHG-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(Cl)N=CC(C)=C1
Synonyms:
  • 2-Chloro-5-Methyl-3-Pyridineboronic Acid
  • 2-Chloro-5-methylpyridine-3-boronic acid
  • B-(2-Chloro-5-methyl-3-pyridinyl)boronic acid
  • Boronic acid, (2-chloro-5-methyl-3-pyridinyl)-
  • T6Nj Bg Cbqq E1 [Wln]
  • boronic acid, B-(2-chloro-5-methyl-3-pyridinyl)-
  • (2-Chloro-5-methylpyridin-3-yl)boronic acid
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