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 31872-78-3
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
3-Amino-5-bromo-4-methoxypyridine features a pyridine core functionalized with electron-donating amino and methoxy groups flanking a bromine atom, enabling selective cross-coupling reactions. This scaffold delivers high reactivity in palladium-catalyzed transformations while maintaining bench-stable handling properties under standard conditions.
3-Amino-5-bromo-4-methoxypyridine serves as a versatile building block in medicinal chemistry, enabling efficient construction of functionalized pyridine scaffolds. The amino group facilitates nucleophilic substitution and coupling reactions, while the bromo and methoxy substituents offer orthogonal reactivity for Pd-catalyzed cross-couplings and selective transformations. Its bench-stable nature and compatibility with diverse reaction conditions make it ideal for iterative synthesis of drug candidates and heterocyclic intermediates.
|
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: