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 381248-04-0
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Chloropyridine-3-boronic acid features a boronic acid group positioned ortho to a chlorine atom on a pyridine ring, enabling direct functionalization in cross-coupling reactions. This configuration enhances reactivity in Suzuki-Miyaura processes while maintaining stability under standard conditions. The electron-deficient pyridine ring facilitates controlled coupling with diverse aryl and heteroaryl partners.
2-Chloropyridine-3-boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient C–C bond formation with aryl and heteroaryl halides. The boronic acid functionality exhibits good bench stability and compatibility with diverse reaction conditions, while the ortho-chloropyridine moiety provides a handle for further functionalization via palladium-catalyzed transformations. Its predictable reactivity and ease of purification make it a practical choice for constructing complex heterocyclic scaffolds in medicinal chemistry and materials science applications.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H315-H319-H335
|
|
|
Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: