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 1026201-45-5
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
8-Bromoimidazo[1,2-a]pyridine-2-carboxylic acid features a brominated imidazopyridine core with a carboxylic acid handle, enabling direct conjugation in medicinal chemistry. This scaffold combines electronic modulation via the bromo substituent with synthetic versatility through the carboxylic acid group, supporting efficient derivatization in drug discovery and materials synthesis under standard conditions.
8-Bromoimidazo[1,2-a]pyridine-2-carboxylic acid serves as a versatile building block for constructing biologically relevant heterocyclic scaffolds. Its bromo group enables palladium-catalyzed cross-coupling reactions, while the carboxylic acid facilitates amide bond formation and derivatization. The molecule exhibits bench stability and compatibility with standard purification methods, making it well-suited for iterative synthesis in medicinal chemistry and process 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 : 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: