Date published: 2026-4-29

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3,4-Dimethoxyphenylboronic acid (CAS 122775-35-3)

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Alternate Names:
3,4-Dimethoxybenzeneboronic Acid
Application:
3,4-Dimethoxyphenylboronic acid is a compound for proteomics research use
CAS Number:
122775-35-3
Molecular Weight:
181.98
Molecular Formula:
C8H11BO4
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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3,4-Dimethoxyphenylboronic acid functions as a key reagent in organic synthesis. It acts as a versatile building block for the construction of various biaryl compounds. 3,4-Dimethoxyphenylboronic Acid participates in Suzuki-Miyaura cross-coupling reactions, where it forms a boronate ester intermediate that undergoes transmetalation with an aryl halide, leading to the formation of a new carbon-carbon bond. Through this mechanism, 3,4-Dimethoxyphenylboronic acid enables the efficient and selective formation of complex organic molecules, making it useful for the synthesis of diverse chemical compounds in research and development applications. Its mechanism of action involves the activation of the boron atom, facilitating its coupling with aryl halides to generate biaryl products with high regio- and stereo-selectivity.


3,4-Dimethoxyphenylboronic acid (CAS 122775-35-3) References

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Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

3,4-Dimethoxyphenylboronic acid, 5 g

sc-254537
5 g
$50.00