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Atomfair (2,3-Dihydro-1,4-benzodioxin-6-yl)boronic acid C8H9BO4

Description (2,3-Dihydro-1,4-benzodioxin-6-yl)boronic acid (CAS No. 164014-95-3) is a high-purity boronic acid derivative with the molecular formula C8H9BO4. This compound features a 2,3-dihydro-1,4-benzodioxin scaffold, making it a valuable building block in organic synthesis, particularly for Suzuki-Miyaura cross-coupling reactions. Its boronic acid functional group enables efficient formation of carbon-carbon bonds with aryl or vinyl halides, catalyzed by palladium complexes. The product is supplied as a white to off-white crystalline powder, rigorously tested for purity (typically ??95% by HPLC or NMR), and is ideal for pharmaceutical, agrochemical, and materials science research. Store under inert conditions at 2-8??C to ensure stability.

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Description

Description

(2,3-Dihydro-1,4-benzodioxin-6-yl)boronic acid (CAS No. 164014-95-3) is a high-purity boronic acid derivative with the molecular formula C8H9BO4. This compound features a 2,3-dihydro-1,4-benzodioxin scaffold, making it a valuable building block in organic synthesis, particularly for Suzuki-Miyaura cross-coupling reactions. Its boronic acid functional group enables efficient formation of carbon-carbon bonds with aryl or vinyl halides, catalyzed by palladium complexes. The product is supplied as a white to off-white crystalline powder, rigorously tested for purity (typically ??95% by HPLC or NMR), and is ideal for pharmaceutical, agrochemical, and materials science research. Store under inert conditions at 2-8??C to ensure stability.

  • CAS No: 164014-95-3
  • Molecular Formula: C8H9BO4
  • Molecular Weight: 179.97
  • Exact Mass: 180.0593889
  • Monoisotopic Mass: 180.0593889
  • IUPAC Name: 2,3-dihydro-1,4-benzodioxin-6-ylboronic acid
  • SMILES: B(C1=CC2=C(C=C1)OCCO2)(O)O
  • Synonyms: (2,3-dihydro-1,4-benzodioxin-6-yl)boronic acid, 625-755-9, 1,4-Benzodioxane-6-boronic acid, 164014-95-3, 2,3-dihydro-1,4-benzodioxin-6-ylboronic acid

Application

(2,3-Dihydro-1,4-benzodioxin-6-yl)boronic acid is widely used in palladium-catalyzed cross-coupling reactions to synthesize complex organic molecules, including pharmaceuticals and functional materials. Its benzodioxin core is a privileged structure in drug discovery, often found in compounds with CNS activity. Researchers also employ it to modify polymers or surfaces via boronic acid-mediated conjugation. The compound’s stability and reactivity make it suitable for high-throughput screening and combinatorial chemistry.

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