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CAS 1217500-52-1

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5-Chloro-2-ethoxypyridine-3-boronic acid

Description:
5-Chloro-2-ethoxypyridine-3-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 substituted with a chlorine atom and an ethoxy group, contributing to its unique chemical properties. The boronic acid moiety allows for the formation of stable complexes with diols and plays a crucial role in the development of pharmaceuticals and agrochemicals. Its solubility in polar solvents and moderate stability under standard conditions make it suitable for various synthetic pathways. Additionally, the presence of the chlorine atom can influence the electronic properties of the molecule, potentially affecting its reactivity and interactions with other chemical species. Overall, 5-Chloro-2-ethoxypyridine-3-boronic acid is a valuable compound in synthetic organic chemistry, particularly in the development of complex molecular architectures.
Formula:C7H9BClNO3
Synonyms:
  • 5-Chloro-2-ethoxypyridine-3-boronic acid
  • (5-Chloro-2-ethoxypyridin-3-yl)boronic acid
  • Boronic acid, B-(5-chloro-2-ethoxy-3-pyridinyl)-
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90
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100
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