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 163704-47-0
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2,6-Diisopropyliodobenzene features a sterically hindered aryl iodide core that enhances stability and facilitates selective cross-coupling reactions. The bulky isopropyl groups shield the iodine atom, reducing undesired side processes while enabling efficient palladium-catalyzed transformations under mild conditions. This bench-stable reagent delivers high functional group tolerance and reliable reactivity in complex molecule assembly.
2,6-Diisopropyliodobenzene serves as a robust aryl iodide building block for palladium-catalyzed cross-coupling reactions, offering enhanced stability and reduced homocoupling compared to simpler aryl iodides. The sterically shielded ortho-isopropyl groups minimize unwanted side reactions, enabling high-yielding Suzuki, Stille, and Negishi couplings. Its bench-stable nature facilitates handling and purification, making it well-suited for iterative synthesis in medicinal chemistry and materials science applications.
|
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: