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 29232-39-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2,3-Dibromo-5-methylpyridine features a pyridine core with bromine substituents at the 2 and 3 positions and a methyl group at the 5 position, delivering enhanced reactivity for cross-coupling transformations. The electron-deficient aromatic ring enables efficient palladium-catalyzed coupling, while the sterically accessible site facilitates selective functionalization. This compound serves as a key intermediate in the synthesis of bioactive heterocycles and advanced materials.
2,3-Dibromo-5-methylpyridine serves as a versatile building block for constructing nitrogen-containing heterocycles and functionalized pyridine derivatives. Its ortho-dibromide substitution enables palladium-catalyzed cross-coupling reactions with minimal side reactivity, while the methyl group provides a handle for further oxidation or functionalization. The compound exhibits good bench stability and facilitates efficient purification via standard chromatographic methods, making it well-suited for iterative synthesis in medicinal chemistry and process development workflows.
|
GHS Pictogram :
|
GHS No : GHS05,GHS06
|
|
Signal Word : Danger
|
UN#: 2811
|
|
Class : 6.1
|
Packing Group : Ⅲ
|
|
Hazard Statements : H301-H318
|
|
|
Precautionary Statements : P264-P270-P280-P330-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: