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 882521-63-3
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
7-Bromo-[1,2,4]triazolo[1,5-a]pyridin-2-amine is a bench-stable heterocyclic building block featuring a brominated triazolopyridine core. This nitrogen-rich scaffold integrates readily into transition metal-catalyzed coupling reactions, enabling efficient access to complex functionalized architectures in medicinal chemistry and materials science.
7-Bromo-[1,2,4]triazolo[1,5-a]pyridin-2-amine serves as a versatile building block for constructing bioactive heterocycles, enabling palladium-catalyzed cross-coupling reactions with broad functional group tolerance. Its bromine substituent facilitates efficient derivatization in Suzuki-Miyaura and Buchwald-Hartwig couplings, while the triazolopyridine core provides structural rigidity and enhanced solubility. The compound exhibits excellent bench stability and is readily purified by flash chromatography, making it well-suited for medicinal chemistry campaigns and API intermediate synthesis.
|
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: