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 1261589-82-5
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Methyl 2-(2-bromothiazol-4-yl)acetate features a brominated thiazole ring linked to a methyl ester-functionalized acetic acid moiety. This electrophilic scaffold integrates readily into cross-coupling reactions and serves as a key intermediate in synthesizing bioactive heterocycles. The bromine atom enables palladium-catalyzed transformations, while the ester group offers versatility in derivatization under standard conditions.
Methyl 2-(2-bromothiazol-4-yl)acetate serves as a versatile building block for thiazole-based scaffolds, enabling palladium-catalyzed cross-coupling reactions with broad functional group tolerance. The bromine atom facilitates efficient C–C bond formation, while the ester group offers further derivatization potential. Its bench-stable nature and compatibility with standard synthetic protocols make it a practical choice for constructing medicinally relevant heterocycles in R&D 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-P280-P302+P352
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: