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 3622-23-9
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2,6-Dichloro-1,3-benzothiazole features a rigid, electron-deficient heterocyclic core that enables efficient coupling in cross-coupling reactions. The ortho-chlorine substituents facilitate regioselective functionalization, while the benzothiazole scaffold offers enhanced stability under oxidative conditions. This compound serves as a robust building block for advanced pharmaceutical intermediates and functional materials.
2,6-Dichloro-1,3-benzothiazole serves as a versatile building block in medicinal chemistry and materials science, enabling the construction of complex heterocyclic scaffolds. Its electron-deficient benzothiazole core facilitates electrophilic substitution and transition-metal-catalyzed coupling reactions. The dichloro substituents provide orthogonal reactivity for selective functionalization, enhancing synthetic versatility in API development and advanced material synthesis.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H315-H319-H335
|
|
|
Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: