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 1270921-80-6
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This boronate moiety integrates a phenoxypyridine scaffold, offering enhanced stability and solubility in polar solvents. The electron-deficient pyridine ring facilitates efficient coupling in Suzuki-Miyaura reactions, while the ortho-phenoxyl group provides steric and electronic modulation. Designed for direct use in transition-metal-catalyzed cross-coupling workflows.
(6-Phenoxypyridin-3-yl)boronic acid serves as a versatile building block in Suzuki-Miyaura coupling reactions, enabling efficient construction of biaryl scaffolds. Its phenoxypyridine core provides enhanced stability and solubility compared to simpler arylboronic acids, while the boronic acid group exhibits reliable reactivity with aryl halides under standard catalytic conditions. The molecule functions effectively in late-stage functionalization and is compatible with diverse functional groups, facilitating its use in medicinal chemistry and materials synthesis workflows.
|
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-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: