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 30766-11-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
5-Bromopicolinic acid features a bromine substituent at the pyridine ring's 5-position, delivering enhanced electrophilicity and facilitating cross-coupling reactions. This bench-stable, moisture-tolerant carboxylic acid integrates readily into synthetic sequences requiring halogenated heterocycles, enabling efficient access to functionalized bioactive scaffolds and advanced intermediates in medicinal chemistry.
5-Bromopicolinic acid serves as a versatile building block in synthetic organic chemistry, enabling direct functionalization at the pyridine ring via palladium-catalyzed cross-coupling reactions. Its bromine substituent offers high reactivity in Suzuki, Stille, and Negishi couplings, while the carboxylic acid group provides a handle for derivatization or amide formation. The compound exhibits excellent bench stability and facilitates purification by recrystallization, making it well-suited for iterative synthesis of bioactive heterocycles and pharmaceutical 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: