

QUICK LINKS
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.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
3,4-Dimethoxyphenylboronic acid, 5 g | sc-254537 | 5 g | $50.00 |