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 201935-41-3
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Chloro-5-methoxybenzenesulfonyl chloride features a sulfonyl chloride group flanked by electron-donating methoxy and electron-withdrawing chloro substituents, enabling selective acylation in synthetic workflows. This bench-stable reagent integrates readily into aromatic sulfonation sequences and serves as a key intermediate for functionalized arylsulfonyl derivatives in pharmaceutical development.
2-Chloro-5-methoxybenzenesulfonyl chloride serves as a versatile sulfonylating agent for the efficient introduction of sulfonamide functionalities under mild conditions. Its ortho-chloro and meta-methoxy substituents enhance reactivity while maintaining bench stability, enabling clean coupling with amines and heterocyclic nitrogen nucleophiles. The compound facilitates rapid access to sulfonamide-containing building blocks relevant to medicinal chemistry and agrochemical research, offering predictable regiochemistry and straightforward purification via crystallization or chromatography.
|
GHS Pictogram :
|
GHS No : GHS05
|
|
Signal Word : Danger
|
UN#: 3261
|
|
Class : 8
|
Packing Group : Ⅲ
|
|
Hazard Statements : H314
|
|
|
Precautionary Statements : P260-P264-P280-P301+P330+P331-P304+P340-P363-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: