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 1146290-36-9
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Fluoro-4-nitrobenzene-1-sulfonyl chloride features a fluorine atom at the ortho position and a nitro group at the para position relative to the sulfonyl chloride, creating an electron-deficient aryl system. This combination enhances reactivity in nucleophilic aromatic substitution processes. The sulfonyl chloride moiety enables efficient coupling with amines and alcohols under mild conditions, facilitating the synthesis of sulfonamide and sulfonate derivatives. The molecule exhibits good bench stability and moisture tolerance, simplifying handling in synthetic workflows.
2-Fluoro-4-nitrobenzene-1-sulfonyl chloride serves as a versatile sulfonylating agent for the synthesis of sulfonamide derivatives, enabling efficient functionalization of amines under mild conditions. Its electron-withdrawing nitro and fluorine substituents enhance reactivity while maintaining bench stability, facilitating clean reactions with broad functional group tolerance. The compound is particularly valuable in constructing heterocyclic scaffolds and bioactive intermediates common in medicinal chemistry workflows.
|
GHS Pictogram :
|
GHS No : GHS05
|
|
Signal Word : Danger
|
UN#: 3261
|
|
Class : 8
|
Packing Group : Ⅲ
|
|
Hazard Statements : H302-H314
|
|
|
Precautionary Statements : P260-P264-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P363-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: