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 42877-08-7
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Acetyl-3-bromothiophene features a bromine substituent at the 3-position and an acetyl group at the 2-position on a thiophene core. This electron-deficient heterocycle serves as a key building block for synthesizing functionalized thienyl derivatives in medicinal chemistry and materials science. The bromine enables palladium-catalyzed cross-coupling reactions, while the acetyl moiety offers a handle for further derivatization.
2-Acetyl-3-bromothiophene serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its bromine substituent. The acetyl group provides a handle for further functionalization via nucleophilic or enolization-based transformations. Its bench-stable nature and compatibility with standard reaction conditions make it well-suited for iterative synthesis of biologically relevant thiophene scaffolds.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H317-H319
|
|
|
Precautionary Statements : P261-P264-P270-P272-P280-P302+P352-P330-P362+P364-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: