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CAS 942438-89-3

:

(5-chloro-6-methoxy-3-pyridyl)boronic acid

Description:
(5-Chloro-6-methoxy-3-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 ring, 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 useful in various chemical reactions, including Suzuki coupling reactions in organic synthesis. The presence of the chlorine and methoxy substituents can influence the electronic properties of the molecule, affecting its reactivity and solubility. Typically, compounds like this are utilized in medicinal chemistry and materials science, particularly in the development of pharmaceuticals and agrochemicals. Additionally, the compound's structure allows for potential interactions with biological targets, making it a candidate for further research in drug development. Overall, (5-chloro-6-methoxy-3-pyridyl)boronic acid exemplifies the versatility of boronic acids in synthetic chemistry.
Formula:C6H7BClNO3
InChI:InChI=1/C6H7BClNO3/c1-12-6-5(8)2-4(3-9-6)7(10)11/h2-3,10-11H,1H3
SMILES:COc1c(cc(cn1)B(O)O)Cl
Synonyms:
  • (5-Chloro-6-methoxypyridin-3-yl)boronic acid
  • boronic acid, B-(5-chloro-6-methoxy-3-pyridinyl)-
  • 3-Chloro-2-methoxypyridine-5-boronic acid
  • B-(5-Chloro-6-methoxy-3-pyridinyl)boronic acid
  • 5-chloro-6-methoxy-pyridine-3-boronic acid
  • (5-CHLORO-6-METHOXY-3-PYRIDYL)BORONIC ACID
  • 5-chloro-6-Methoxypyridin-3-yl-3-boronic acid
  • 3-Chloro-2-methoxypyridine-5-boronicaci
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