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 19755-53-4
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Bromo-3-nitropyridine features a strategically positioned bromine and nitro group on the pyridine ring, enabling direct functionalization in cross-coupling and nucleophilic substitution reactions. The electron-deficient heterocycle enhances reactivity toward palladium-catalyzed transformations, while maintaining stability under standard bench conditions.
2-Bromo-3-nitropyridine serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its stable bromine functionality. The nitro group provides a handle for selective reduction and further functionalization, while the pyridine core offers inherent polarity and coordination capability. Its bench stability and compatibility with standard reaction conditions facilitate efficient access to substituted pyridine scaffolds relevant to medicinal chemistry and agrochemical development.
|
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: