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 426463-09-4
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Chloro-5-iodopyridin-3-amine features a halogenated pyridine core with complementary chlorine and iodine substituents at the 2- and 5-positions, respectively, enabling selective cross-coupling reactions. The amine group at the 3-position provides a reactive handle for derivatization, while the molecule exhibits stability under standard bench conditions. This combination supports efficient access to complex heterocyclic architectures in medicinal chemistry and materials science applications.
2-Chloro-5-iodopyridin-3-amine serves as a versatile building block for the construction of functionalized pyridine scaffolds in medicinal chemistry and materials science. Its complementary halogenation pattern enables sequential cross-coupling reactions via palladium catalysis, facilitating efficient access to biaryl and heterocyclic architectures. The compound exhibits good bench stability and is compatible with standard purification techniques, making it well-suited for iterative synthesis workflows in API development and library generation.
|
GHS Pictogram :
|
GHS No : GHS05,GHS07
|
|
Signal Word : Danger
|
UN#: 3259
|
|
Class : 8
|
Packing Group : Ⅲ
|
|
Hazard Statements : H302-H318
|
|
|
Precautionary Statements : P264-P270-P280-P330-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: