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 885521-46-0
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
3-Iodo-1H-indazole-5-carboxylic acid features a sterically accessible indazole core functionalized with iodine and carboxylic acid groups at the 3- and 5-positions, respectively. This combination enables direct coupling in palladium-catalyzed cross-coupling reactions, offering efficient access to bioactive indazole derivatives under standard conditions. The molecule exhibits excellent stability and solubility in common organic solvents, facilitating use in synthetic workflows.
3-Iodo-1H-indazole-5-carboxylic acid serves as a versatile building block for the synthesis of indazole-based pharmaceuticals and functional materials. The iodine substituent enables palladium-catalyzed cross-coupling reactions, while the carboxylic acid group offers direct derivatization potential via amide formation or esterification. Its stability under standard bench conditions and compatibility with diverse reaction environments facilitate efficient integration into multi-step synthetic sequences.
|
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: