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CAS 850864-59-4

:

B-(5-Bromo-2-methoxy-3-pyridinyl)boronic acid

Description:
B-(5-Bromo-2-methoxy-3-pyridinyl)boronic acid, with the CAS number 850864-59-4, is an organoboron compound characterized by the presence of a boronic acid functional group attached to a pyridine ring that is substituted with a bromine atom and a methoxy group. This compound typically exhibits properties such as being a white to off-white solid, soluble in polar organic solvents, and possessing moderate stability under standard conditions. The boronic acid moiety allows for participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in organic synthesis, particularly in the formation of carbon-carbon bonds. Additionally, the presence of the bromine and methoxy substituents can influence its reactivity and solubility, as well as its potential applications in medicinal chemistry and material science. The compound may also exhibit biological activity, which can be explored in various research contexts, particularly in the development of pharmaceuticals. Proper handling and storage conditions are essential due to the potential reactivity of boronic acids.
Formula:C6H7BBrNO3
InChI:InChI=1S/C6H7BBrNO3/c1-12-6-5(7(10)11)2-4(8)3-9-6/h2-3,10-11H,1H3
InChI key:InChIKey=KIMPFSRSIJTVLK-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(OC)N=CC(Br)=C1
Synonyms:
  • 2-Chloro-5-formylbenzeneboronic acid
  • 2-Chloro-5-formylphenylboronic acid
  • B-(2-Chloro-5-formylphenyl)boronic acid
  • B-(5-Bromo-2-methoxy-3-pyridinyl)boronic acid
  • Boronic acid, (5-bromo-2-methoxy-3-pyridinyl)-
  • Boronic acid, B-(2-chloro-5-formylphenyl)-
  • Boronic acid, B-(5-bromo-2-methoxy-3-pyridinyl)-
  • Vhr Dg Cbqq
  • [5-Bromo-2-methoxy-3-pyridinyl]boronic acid
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