Cas no 1799426-61-1 (5-Methoxy-6-methylpyridin-3-ylboronic acid)

5-Methoxy-6-methylpyridin-3-ylboronic acid is a boronic acid derivative commonly employed as a key intermediate in Suzuki-Miyaura cross-coupling reactions, a widely utilized method for forming carbon-carbon bonds in organic synthesis. Its pyridine core, substituted with methoxy and methyl groups, enhances its stability and reactivity in palladium-catalyzed transformations. This compound is particularly valuable in pharmaceutical and agrochemical research, where it facilitates the construction of complex heterocyclic scaffolds. The boronic acid functionality ensures compatibility with a broad range of aryl and heteroaryl halides, enabling efficient synthesis of biaryl structures. Its well-defined reactivity profile and moderate stability under standard conditions make it a reliable reagent for targeted synthetic applications.
5-Methoxy-6-methylpyridin-3-ylboronic acid structure
1799426-61-1 structure
Product Name:5-Methoxy-6-methylpyridin-3-ylboronic acid
CAS No:1799426-61-1
MF:C7H10BNO3
MW:166.970201969147
CID:4935132
Update Time:2026-02-27

5-Methoxy-6-methylpyridin-3-ylboronic acid Chemical and Physical Properties

Names and Identifiers

    • 3-Methoxy-2-methylpyridine-5-boronic acid
    • 5-methoxy-6-methylpyridin-3-ylboronic acid
    • 5-Methoxy-6-methylpyridin-3-ylboronic acid
    • Inchi: 1S/C7H10BNO3/c1-5-7(12-2)3-6(4-9-5)8(10)11/h3-4,10-11H,1-2H3
    • InChI Key: ZVIHBDCSPMIZBC-UHFFFAOYSA-N
    • SMILES: O(C)C1=CC(B(O)O)=CN=C1C

Computed Properties

  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 2
  • Complexity: 145
  • Topological Polar Surface Area: 62.6

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