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 889676-37-3
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
6-Bromonicotinamide features a bromine substituent at the pyridine ring's 6-position, enabling direct functionalization in cross-coupling reactions. The amide group provides enhanced solubility and stability compared to nitrile precursors. This bifunctional scaffold integrates readily into pharmaceutical intermediates and advanced materials.
6-Bromonicotinamide serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the pyridine ring via palladium-catalyzed cross-coupling reactions. Its bromine substituent exhibits high reactivity in Suzuki, Stille, and Negishi transformations, while the amide group provides polarity and hydrogen-bonding capacity for improved solubility and target engagement. The compound demonstrates excellent bench stability and is readily purified by flash chromatography or recrystallization, making it well-suited for iterative synthesis of heterocyclic scaffolds and API 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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: