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 13958-99-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
3-Bromoisonicotinamide features a bromine substituent at the pyridine ring's 3-position, enhancing electrophilic reactivity for cross-coupling applications. This bench-stable amide integrates readily into pharmaceutical intermediates and functional materials, offering predictable regiochemistry in Suzuki-Miyaura and Buchwald-Hartwig reactions.
3-Bromoisonicotinamide serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions for the construction of biaryl and heteroaryl scaffolds. Its bromine substituent facilitates reliable Suzuki, Stille, and Negishi couplings, while the amide group provides hydrogen-bonding capacity and metabolic stability. The compound exhibits excellent bench stability and is compatible with a wide range of functional groups, making it well-suited for iterative synthesis campaigns and API development workflows.
|
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 : P233-P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: