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 655-26-5
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This trifluoromethyl ketone features a 3-bromophenyl group attached to a reactive α,α,α-trifluoroacetone scaffold. The electron-withdrawing trifluoromethyl moiety enhances electrophilicity at the carbonyl carbon, enabling efficient nucleophilic addition reactions. Bench-stable and moisture-tolerant, it serves as a key building block for pharmaceutical intermediates and functionalized aromatics in synthetic chemistry workflows.
1-(3-bromophenyl)-2,2,2-trifluoroethan-1-one serves as a versatile building block for the synthesis of trifluoromethylated aryl ketones and heterocyclic scaffolds. Its stability under standard reaction conditions and compatibility with palladium-catalyzed cross-coupling reactions enable efficient access to functionalized biaryl systems. The trifluoromethyl ketone moiety facilitates nucleophilic addition and acts as a key electrophilic handle in medicinal chemistry lead optimization.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H315-H319-H335
|
|
|
Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: