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 188057-26-3
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
6-Chloro-2-iodopyridin-3-ol features a sterically accessible pyridin-3-ol core with complementary halogen handles: a chlorine at C6 and an iodine at C2. This arrangement enables selective cross-coupling reactions, particularly in late-stage functionalization of heterocyclic scaffolds. The phenolic hydroxyl group enhances solubility and provides a handle for derivatization, while the electron-deficient ring system supports efficient palladium-catalyzed transformations under standard conditions.
6-Chloro-2-iodopyridin-3-ol serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its complementary halogen reactivity. The iodide group facilitates efficient C–C and C–heteroatom bond formation, while the chloro and hydroxyl substituents offer orthogonal functionalization potential. This compound exhibits bench stability and is compatible with standard purification methods, making it well-suited for modular synthesis of bioactive heterocycles 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: