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 406233-31-6
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
4-Fluoro-3-nitrobenzenesulfonamide features a sulfonamide group flanked by electron-withdrawing fluorine and nitro substituents, enhancing its reactivity in nucleophilic aromatic substitution. This configuration imparts high stability under standard conditions while enabling selective derivatization in synthetic routes requiring activated aryl systems.
4-Fluoro-3-nitrobenzenesulfonamide serves as a versatile building block in medicinal chemistry, enabling efficient access to functionalized aromatic scaffolds. The ortho-directed nitro and fluoro groups facilitate regioselective substitutions, while the sulfonamide moiety offers hydrogen-bonding capacity and metabolic stability. Its bench-stable nature and compatibility with standard coupling reactions make it suitable for iterative synthesis of complex heterocycles and API intermediates.
|
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: