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 177363-10-9
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
1-Fluoro-2-iodo-4-nitrobenzene features a trifunctional aryl scaffold with orthogonal reactivity, enabling sequential cross-coupling processes. The fluorine atom facilitates palladium-catalyzed substitutions, while the iodine group serves as a high-efficiency coupling handle. The para-nitro substituent enhances electrophilicity and provides synthetic leverage for downstream functionalization. This compound offers predictable regioselectivity in transition metal-mediated transformations under standard conditions.
1-Fluoro-2-iodo-4-nitrobenzene serves as a versatile building block in transition-metal-catalyzed cross-coupling reactions, enabling efficient construction of substituted aryl scaffolds. The ortho-iodo and fluoro groups provide complementary sites for sequential functionalization, while the electron-withdrawing nitro group enhances reactivity in palladium-catalyzed couplings. Its bench-stable nature and high functional group tolerance make it ideal for multi-step 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: