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 916792-62-6
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
3-Fluoro-2-iodobenzonitrile features a fluorine atom at the meta position and an iodine substituent at the ortho position relative to the nitrile group, enabling efficient palladium-catalyzed cross-coupling reactions. The electron-withdrawing nitrile and iodine moieties facilitate regioselective transformations in synthetic sequences. This bench-stable aryl iodide integrates readily into complex molecular architectures under standard conditions.
3-Fluoro-2-iodobenzonitrile serves as a versatile building block in transition-metal-catalyzed cross-coupling reactions, enabling efficient construction of biaryl scaffolds. The ortho-iodo group exhibits high reactivity in palladium-catalyzed couplings, while the meta-fluoro and nitrile functionalities provide orthogonal handles for further functionalization. Its bench-stable nature and compatibility with diverse reaction conditions make it well-suited for medicinal chemistry and process development workflows.
|
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: