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 182344-57-6
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
4-Bromo-2-chlorobenzo[d]thiazole features a fused heterocyclic core with strategically positioned halogens, enabling direct functionalization in cross-coupling reactions. The electron-deficient thiazole ring facilitates nucleophilic substitution, while the bromo and chloro substituents offer orthogonal reactivity for sequential derivatization. This compound serves as a robust scaffold in medicinal chemistry and materials science.
4-Bromo-2-chlorobenzo[d]thiazole serves as a versatile building block in medicinal chemistry and materials science, enabling efficient construction of biologically active heterocycles. Its dual halogenation pattern facilitates palladium-catalyzed cross-coupling reactions with high chemoselectivity and functional group tolerance. The molecule exhibits excellent bench stability and ease of purification, making it well-suited for iterative synthesis workflows and scale-up applications in API development.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H315-H319-H335
|
|
|
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: