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 39891-12-8
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
5-Bromo-3-pyridylacetic acid features a brominated pyridine ring linked to a carboxylic acid-bearing acetic side chain, enabling direct incorporation into bioactive molecule scaffolds. The electron-deficient pyridine core enhances reactivity in cross-coupling and functionalization reactions, while the pendant carboxyl group provides a handle for amide bond formation or metal chelation. This structure supports synthetic access to pharmaceutical intermediates and ligands requiring halogenated heterocyclic motifs under standard conditions.
5-Bromo-3-pyridylacetic acid serves as a versatile building block for constructing bioactive heterocycles and pharmaceutical intermediates. Its brominated pyridine core enables efficient Pd-catalyzed cross-coupling reactions, while the carboxylic acid group facilitates direct derivatization or amidation. The compound exhibits good bench stability and compatibility with standard synthetic workflows, enabling straightforward incorporation into complex molecular architectures.
|
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: