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 2369772-11-0
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This boronate ester features a 4-chloro-2-methoxy-5-pyridyl scaffold, enabling efficient cross-coupling under standard conditions. The tetramethyl-1,3,2-dioxaborolane moiety provides enhanced stability and reactivity, facilitating direct incorporation into complex molecular architectures via palladium-catalyzed transformations.
4-Chloro-2-methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine serves as a versatile Suzuki-Miyaura coupling building block, enabling efficient C–C bond formation under mild conditions. The boronate ester group exhibits excellent stability and functional group tolerance, while the chloropyridine moiety provides a reactive handle for palladium-catalyzed cross-coupling. Its bench-stable nature and compatibility with diverse reaction partners make it ideal for constructing complex heterocyclic scaffolds in medicinal chemistry and materials science applications.
|
GHS Pictogram :
N/A
|
GHS No : N/A
|
|
Signal Word : N/A
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : N/A
|
|
|
Precautionary Statements : N/A
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: