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CAS 1072945-98-2

:

B-(2-Chloro-5-methoxy-4-pyridinyl)boronic acid

Description:
B-(2-Chloro-5-methoxy-4-pyridinyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a pyridine ring. 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 presence of the chloro and methoxy substituents on the pyridine ring can influence its reactivity and solubility, making it useful in various chemical reactions, particularly in Suzuki coupling reactions, which are pivotal in organic synthesis for forming carbon-carbon bonds. Additionally, boronic acids are known for their ability to form reversible complexes with diols, which can be exploited in various applications, including drug delivery and sensor technology. The compound's specific reactivity and applications may vary based on its structural features, making it a valuable intermediate in the synthesis of pharmaceuticals and agrochemicals.
Formula:C6H7BClNO3
InChI:InChI=1S/C6H7BClNO3/c1-12-5-3-9-6(8)2-4(5)7(10)11/h2-3,10-11H,1H3
InChI key:InChIKey=RIJYQJUSSTXMRQ-UHFFFAOYSA-N
SMILES:B(O)(O)C=1C(OC)=CN=C(Cl)C1
Synonyms:
  • 2-Chloro-5-methoxypyridine-4-boronic acid
  • B-(2-Chloro-5-methoxy-4-pyridinyl)boronic acid
  • (2-Chloro-5-methoxypyridin-4-yl)boronic acid
  • Boronic acid, B-(2-chloro-5-methoxy-4-pyridinyl)-
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