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 1204112-62-8
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This boronate moiety integrates seamlessly into Suzuki-Miyaura cross-coupling reactions, offering enhanced reactivity and stability under standard conditions. The ortho-aminopyridyl group enables efficient coordination in catalytic systems, facilitating selective functionalization of heteroaromatic scaffolds with minimal side-product formation.
(2-Aminopyridin-3-yl)boronic acid serves as a versatile building block in transition-metal-catalyzed cross-coupling reactions, enabling efficient C–C bond formation under mild conditions. Its ortho-amino functionality enhances coordination to palladium catalysts and improves reaction efficiency in Suzuki-Miyaura coupling. The boronic acid moiety offers excellent bench stability, facile purification, and compatibility with diverse functional groups, making it ideal for constructing biologically relevant 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 : 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: