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CAS 94838-88-7

:

(6-formyl-1,3-benzodioxol-5-yl)boronic acid

Description:
(6-formyl-1,3-benzodioxol-5-yl)boronic acid, with the CAS number 94838-88-7, is an organic compound that features a boronic acid functional group attached to a benzodioxole moiety. This compound is characterized by its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of the formyl group contributes to its reactivity, allowing it to participate in condensation reactions and other transformations. The benzodioxole structure imparts unique electronic properties, enhancing its potential as a building block in the synthesis of more complex molecules. Additionally, boronic acids are known for their role in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds. The compound's solubility and stability can vary depending on the solvent and conditions, and it is typically handled with care due to the potential reactivity of the boronic acid group. Overall, (6-formyl-1,3-benzodioxol-5-yl)boronic acid is a versatile compound with significant implications in chemical research and development.
Formula:C8H7BO5
InChI:InChI=1/C8H7BO5/c10-3-5-1-7-8(14-4-13-7)2-6(5)9(11)12/h1-3,11-12H,4H2
SMILES:c1c(C=O)c(cc2c1OCO2)B(O)O
Synonyms:
  • boronic acid, B-(6-formyl-1,3-benzodioxol-5-yl)-
  • (6-Formyl-1,3-benzodioxol-5-yl)boronic acid
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