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 181124-40-3
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Benzo[d]thiazole-6-sulfonyl chloride delivers a reactive sulfonyl chloride handle positioned ortho to the heterocyclic core, enabling direct conjugation with nucleophiles under mild conditions. This electron-deficient scaffold integrates readily into bioactive architectures, offering enhanced metabolic stability and solubility in polar media.
Benzo[d]thiazole-6-sulfonyl chloride serves as a versatile building block for constructing sulfonamide-containing heterocycles, enabling efficient incorporation into pharmaceutical scaffolds. Its reactive sulfonyl chloride group facilitates direct amidation and nucleophilic substitution under mild conditions, offering high functional group tolerance and bench stability. Widely employed in medicinal chemistry, it functions as a key intermediate in the synthesis of kinase inhibitors and other bioactive compounds, with predictable reactivity profiles suitable for both small-scale exploration and process-scale applications.
|
GHS Pictogram :
|
GHS No : GHS05
|
|
Signal Word : Danger
|
UN#: 1759
|
|
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: