Lot numbers can be found on the outside label of a product:
Please log in for operation!
*For research and further manufacturing use only, not for direct human use.
Structure of 219834-95-4
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This boronic acid features a methoxy-substituted naphthyl group, delivering enhanced solubility and stability in polar solvents. The electron-donating methoxy moiety improves reaction kinetics in Suzuki-Miyaura couplings. Bench-stable under standard conditions, it integrates seamlessly into synthetic workflows requiring reliable coupling efficiency and minimal handling complexity.
(4-methoxy-1-naphthyl)boronic acid serves as a reliable building block for Suzuki-Miyaura cross-coupling reactions, enabling efficient C–C bond formation under mild conditions. Its naphthyl scaffold provides enhanced π-conjugation and stability, while the methoxy group offers moderate electron-donating character and improved solubility. The boronic acid functions reliably in diverse reaction environments, facilitating access to complex aromatic architectures with high reproducibility and ease of purification.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H315-H319-H335
|
|
|
Precautionary Statements : P261-P280-P302+P352
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: