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 161091-49-2
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
3-Bromo-5,6-dimethylpyridin-2-amine features a brominated pyridine core with two methyl groups at the 5 and 6 positions, delivering enhanced electron density and steric bulk. This configuration supports efficient coupling reactions in transition-metal-catalyzed transformations, particularly in pharmaceutical and agrochemical synthesis where regioselective functionalization is critical. The molecule exhibits excellent stability under standard conditions and facilitates rapid diversification of heterocyclic scaffolds.
3-Bromo-5,6-dimethylpyridin-2-amine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its bromine substituent and electron-rich pyridine core. The dimethyl groups enhance stability and modulate reactivity, while the amino group provides a handle for derivatization. Its bench-stable nature and compatibility with standard coupling protocols facilitate efficient construction of complex heterocyclic scaffolds.
|
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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: