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 654067-65-9
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This boronic acid features a di-p-tolylamino-substituted phenyl scaffold, delivering enhanced solubility and stability in organic media. The electron-rich aryl system facilitates efficient Suzuki-Miyaura cross-coupling reactions under mild conditions. Designed for synthetic versatility, it integrates seamlessly into complex molecular architectures requiring robust C–C bond formation.
(4-(Di-p-tolylamino)phenyl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient C–C bond formation under mild conditions. Its stability, ease of handling, and tolerance to diverse functional groups make it ideal for constructing biaryl scaffolds in pharmaceutical and materials synthesis. The di-p-tolylamino moiety enhances solubility and electronic modulation, facilitating predictable reactivity in iterative coupling strategies.
|
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: