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CAS 164014-95-3

:

1,4-Benzodioxane-6-boronic acid

Description:
1,4-Benzodioxane-6-boronic acid, identified by its CAS number 164014-95-3, is an organic compound that features a benzodioxane core with a boronic acid functional group. This compound typically exhibits a white to off-white crystalline appearance and is soluble in polar solvents such as water and alcohols, owing to the presence of the boronic acid group, which can engage in hydrogen bonding. The boronic acid moiety allows for potential applications in organic synthesis, particularly in Suzuki coupling reactions, where it can act as a reagent for forming carbon-carbon bonds. Additionally, the compound may exhibit properties that make it useful in medicinal chemistry, particularly in the development of pharmaceuticals targeting specific biological pathways. Its structural characteristics, including the fused dioxane ring, contribute to its chemical reactivity and stability. As with many boronic acids, it is important to handle this compound with care, as it may be sensitive to moisture and air, which can affect its reactivity and shelf life.
Formula:C8H9BO4
InChI:InChI=1/C8H9BO4/c10-9(11)6-1-2-7-8(5-6)13-4-3-12-7/h1-2,5,10-11H,3-4H2
SMILES:c1cc2c(cc1B(O)O)OCCO2
Synonyms:
  • (1,4-Benzodioxan-6-Yl)Boronic Acid
  • 2,3-Dihydrobenzo[B][1,4]Dioxin-6-Ylboronic Acid
  • 2,3-Dihydro-1,4-Benzodioxin-6-Ylboronic Acid
  • 3,4-(Ethylenedioxy)Benzeneboronic Acid
  • 1,4-Benzodioxan-6-Boronic Acid
  • 2,3-Dihydro-1,4-benzodioxine-6-boronic acid
  • 2,3-dihydro �Cbenzo[b][1.4]dioxin-6-yl-6-boronic acid
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