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 328955-61-9
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
6-Bromo-4-(trifluoromethyl)quinolin-2(1H)-one is a fluorinated quinolinone scaffold featuring a bromine substituent at the 6-position and a trifluoromethyl group at the 4-position. This electron-deficient heterocycle serves as a strategic building block in medicinal chemistry, enabling direct C–H functionalization and facilitating access to complex polycyclic architectures through palladium-catalyzed cross-coupling reactions.
6-Bromo-4-(trifluoromethyl)quinolin-2(1H)-one serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its bromo substituent and electron-deficient quinolinone core. The trifluoromethyl group enhances metabolic stability and lipophilicity, while the keto functionality supports further functionalization. This compound exhibits good bench stability and is compatible with standard purification methods, facilitating integration into multi-step synthesis workflows for bioactive heterocycles.
|
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: