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 88675-31-4
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This bromoketone features a fluorophenyl moiety flanked by a phenyl group and a reactive carbonyl, enabling direct functionalization in cross-coupling processes. The electron-deficient aryl system enhances reactivity, while the bromine atom provides a handle for palladium-catalyzed transformations. Bench-stable under standard conditions, it integrates efficiently into complex molecular architectures.
2-Bromo-1-(4-fluorophenyl)-2-phenylethan-1-one serves as a versatile building block in synthetic organic chemistry, enabling efficient construction of biaryl and heterocyclic scaffolds. Its brominated ketone functionality supports palladium-catalyzed cross-coupling reactions, while the fluorophenyl and phenyl groups provide orthogonal reactivity and structural rigidity. The compound exhibits good bench stability and facilitates straightforward purification, making it well-suited for iterative synthesis workflows in medicinal chemistry and process development.
|
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: