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 10531-41-6
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Bromo-1-(thiophen-2-yl)ethanone features a bromine-substituted ketone moiety flanked by a thiophene ring, enabling direct incorporation into cross-coupling reactions. This bench-stable reagent delivers efficient access to functionalized aryl ketones under standard conditions.
2-Bromo-1-(thiophen-2-yl)ethanone serves as a versatile building block for heterocyclic synthesis, enabling efficient access to thiophene-fused scaffolds via nucleophilic substitution and coupling reactions. The α-bromo ketone functionality facilitates C–C bond formation under mild conditions, while the thiophene ring provides structural rigidity and electronic modulation. Bench-stable and compatible with standard purification methods, it functions reliably in multistep synthetic sequences for medicinal chemistry and materials science applications.
|
GHS Pictogram :
|
GHS No : GHS05,GHS07
|
|
Signal Word : Danger
|
UN#: 3261
|
|
Class : 8
|
Packing Group : Ⅱ
|
|
Hazard Statements : H302-H314-H317
|
|
|
Precautionary Statements : P260-P264-P270-P280-P301+P330+P331-P304+P340-P330-P363-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: