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 590417-67-7
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This boronate moiety integrates seamlessly into Suzuki-Miyaura cross-coupling reactions, delivering functionalized heteroaryl scaffolds with high efficiency. The ortho-methyl group enhances stability and modulates reactivity, while the thiazole ring provides a rigid, electron-deficient platform for downstream derivatization. Bench-stable under standard conditions, this reagent simplifies access to complex bioactive architectures in medicinal chemistry and materials science workflows.
(2-Methylbenzo[d]thiazol-5-yl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl architectures. Its stability under ambient conditions and compatibility with diverse functional groups facilitate straightforward purification and integration into complex molecular frameworks. The boronic acid moiety enables reliable C–C bond formation, making it particularly valuable for synthesizing heterocyclic scaffolds relevant to medicinal chemistry and materials science.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H319
|
|
|
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: