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 1649470-53-0
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
5-Fluoro-4-iodopyridin-2-amine features a strategically positioned fluorine and iodine substituent on the pyridine ring, enabling facile cross-coupling reactions. The electron-deficient aromatic core pairs with the nucleophilic amine group to deliver high reactivity in palladium-catalyzed transformations. This compound serves as a key building block for bioactive heterocycles and pharmaceutical intermediates under standard coupling conditions.
5-Fluoro-4-iodopyridin-2-amine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its iodine functionality. The fluorinated pyridine scaffold provides enhanced metabolic stability and modulates electronic properties, while the amine group facilitates further derivatization. This compound exhibits good bench stability and is compatible with standard purification protocols, making it well-suited for iterative synthesis of heterocyclic scaffolds and API intermediates.
|
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: