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CAS 475275-69-5

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(5-chloro-2-methoxy-4-pyridyl)boronic acid

Description:
(5-Chloro-2-methoxy-4-pyridyl)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 methoxy group at specific positions on the pyridine, which contribute to its chemical reactivity and potential applications. The boronic acid moiety is known for its ability to form reversible covalent bonds with diols, making it valuable in various chemical reactions, including Suzuki coupling, which is widely used in organic synthesis. The presence of the chlorine and methoxy substituents can influence the compound's solubility, stability, and reactivity, allowing for diverse applications in medicinal chemistry and materials science. Additionally, the compound may exhibit biological activity, making it of interest in pharmaceutical research. Its molecular structure and functional groups can be analyzed using techniques such as NMR spectroscopy and mass spectrometry, providing insights into its properties and potential uses in drug development and other fields.
Formula:C6H7BClNO3
InChI:InChI=1/C6H7BClNO3/c1-12-6-2-4(7(10)11)5(8)3-9-6/h2-3,10-11H,1H3
SMILES:COc1cc(c(cn1)Cl)B(O)O
Synonyms:
  • (5-Chloro-2-methoxy-4-pyridinyl)boronic acid
  • (5-Chloro-2-methoxypyridin-4-yl)boronic acid
  • boronic acid, B-(5-chloro-2-methoxy-4-pyridinyl)-
  • 5-Chloro-2-methoxypyridine-4-boronicacid
  • 5-Chloro-2-methoxypyridine-4-boronic acid
  • 5-Chloro-2-Methoxypyridin-4-Ylboronic Acid
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