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 1202237-88-4
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Ethyl 5-bromothiazole-2-carboxylate features a brominated thiazole core that enables direct functionalization in cross-coupling reactions. This bench-stable, moisture-tolerant reagent integrates readily into synthetic sequences requiring halogen-directed diversification. The ester group facilitates purification and downstream derivatization, while the electron-deficient heterocycle enhances reactivity in palladium-catalyzed transformations.
Ethyl 5-bromothiazole-2-carboxylate serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions for the construction of thiazole-based scaffolds. The bromine substituent facilitates efficient functionalization via Suzuki, Stille, or Negishi coupling, while the ester group supports further derivatization. Bench-stable and compatible with standard reaction conditions, it functions reliably in medicinal chemistry and process development workflows.
|
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: