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 70315-70-7
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
3-Iodo-6-nitro-1H-indazole features a fused bicyclic core bearing iodine and nitro groups at distinct positions, enabling selective cross-coupling reactions. The electron-deficient indazole scaffold enhances reactivity in palladium-catalyzed transformations, while the bench-stable nature supports reliable handling in synthetic workflows.
3-Iodo-6-nitro-1H-indazole serves as a versatile building block for transition-metal-catalyzed cross-coupling reactions, enabling efficient construction of biaryl and heteroaryl architectures. The iodide moiety facilitates palladium-catalyzed coupling with boronic acids, stannanes, and other nucleophiles under standard conditions. The 6-nitro group enhances electrophilicity at C5 and supports sequential functionalization, while the indazole core provides structural rigidity and hydrogen-bonding capacity relevant to medicinal chemistry scaffolds. Bench-stable and amenable to purification by flash chromatography, it is well-suited for iterative synthesis workflows in API development.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302
|
|
|
Precautionary Statements : P264-P270-P330-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: