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 18494-87-6
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Benzothiophene-3-sulfonyl chloride features a reactive sulfonyl chloride group flanked by an electron-rich benzothiophene core, enabling direct incorporation into sulfonamide derivatives. This bench-stable reagent facilitates efficient coupling under mild conditions, delivering high-yield functionalization in synthetic and medicinal chemistry workflows.
Benzothiophene-3-sulfonyl chloride serves as a versatile acylating agent for the introduction of a benzothiophene-3-sulfonyl group into diverse molecular scaffolds. It enables efficient formation of sulfonamides and sulfonate esters under mild conditions, demonstrating good bench stability and compatibility with common functional groups. This reagent facilitates access to key intermediates in medicinal chemistry campaigns, particularly in kinase inhibitor and GPCR-targeted drug discovery, where the sulfonyl moiety contributes to target binding affinity and metabolic stability.
|
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-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: