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CAS 503184-35-8

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B-(6-Methoxy-4-methyl-3-pyridinyl)boronic acid

Description:
B-(6-Methoxy-4-methyl-3-pyridinyl)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 methoxy group and a methyl group on the pyridine, which contribute to its unique chemical properties. It is typically used in organic synthesis, particularly in Suzuki coupling reactions, where it serves as a key reagent for forming carbon-carbon bonds. The boronic acid moiety allows for reversible binding with diols, making it useful in various applications, including drug development and materials science. The compound is generally stable under standard conditions but may require careful handling due to its reactivity with moisture and air. Its solubility in organic solvents and moderate polarity make it suitable for various synthetic applications. Additionally, the presence of the pyridine ring can influence its biological activity, potentially making it a candidate for pharmaceutical research. Overall, B-(6-Methoxy-4-methyl-3-pyridinyl)boronic acid is a versatile compound with significant utility in both academic and industrial chemistry.
Formula:C7H10BNO3
InChI:InChI=1S/C7H10BNO3/c1-5-3-7(12-2)9-4-6(5)8(10)11/h3-4,10-11H,1-2H3
InChI key:InChIKey=RLWTZURPSVMYGG-UHFFFAOYSA-N
SMILES:B(O)(O)C=1C(C)=CC(OC)=NC1
Synonyms:
  • (2-Methoxy-4-methylpyridin-5-yl)boronic acid
  • (6-Methoxy-4-methylpyridin-3-yl)boronic acid
  • 2-Methoxy-4-methylpyridine-5-boronic acid
  • 6-Methoxy-4-Methylpyridin-3-Ylboronic Acid
  • 6-Methoxy-4-methylpyridine-3-boronic acid
  • B-(6-Methoxy-4-methyl-3-pyridinyl)boronic acid
  • Boronic acid, (6-methoxy-4-methyl-3-pyridinyl)-
  • boronic acid, B-(6-methoxy-4-methyl-3-pyridinyl)-
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