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 188057-49-0
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
5-Bromo-2-iodopyridin-3-ol features a pyridin-3-ol core substituted with bromo and iodo groups at the 5- and 2-positions, respectively. This electron-deficient heterocycle enables direct functionalization in cross-coupling reactions. The phenolic hydroxyl group enhances solubility and provides a handle for derivatization. Bench-stable under standard conditions, it serves as a key building block in medicinal chemistry and materials synthesis.
5-Bromo-2-iodopyridin-3-ol serves as a versatile building block for late-stage functionalization and cross-coupling reactions in medicinal chemistry. Its dual halogenation pattern enables sequential Pd-catalyzed couplings with high chemoselectivity, while the phenolic hydroxyl group supports derivatization and metal coordination. The compound exhibits excellent bench stability and facilitates purification via recrystallization, making it well-suited for scalable 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: