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 349-71-3
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
4-Acetamido-3-fluorobenzenesulfonyl chloride features a fluorinated aromatic ring paired with an electron-withdrawing sulfonyl chloride group, enabling selective acylation in synthetic workflows. The acetamido substituent enhances solubility and modulates reactivity, while the sulfonyl chloride moiety facilitates efficient coupling under mild conditions. This bench-stable reagent delivers precise functionalization in pharmaceutical intermediates and specialty materials.
4-Acetamido-3-fluorobenzenesulfonyl chloride serves as a versatile sulfonylating agent for the selective introduction of sulfonamide groups into pharmaceutical intermediates. Its ortho-fluoro and acetamido substituents enhance reactivity and functional group tolerance, enabling efficient coupling with amines under mild conditions. The compound exhibits excellent bench stability and facilitates straightforward purification, making it well-suited for scalable synthesis of bioactive heterocycles and API precursors.
|
GHS Pictogram :
|
GHS No : GHS05,GHS07
|
|
Signal Word : Danger
|
UN#: 3261
|
|
Class : 8
|
Packing Group : Ⅲ
|
|
Hazard Statements : H302-H312-H314-H332-H335
|
|
|
Precautionary Statements : P260-P261-P264-P270-P271-P280-P301+P330+P331-P302+P352-P304+P340-P330-P362+P364-P363-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: