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 1219130-55-8
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This boronate-functionalized quinolinone integrates readily into Suzuki-Miyaura coupling reactions under standard conditions. The tetramethylboronate moiety enhances stability and solubility, enabling efficient cross-coupling with aryl halides. The electron-deficient quinolinone core supports targeted derivatization in medicinal chemistry applications.
8-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)quinolin-2(1H)-one serves as a versatile boronate building block for palladium-catalyzed cross-coupling reactions. Its quinolinone core enables efficient incorporation into biologically relevant scaffolds, while the stable tetramethylborolane group facilitates mild, selective coupling under standard conditions. The compound exhibits excellent bench stability and compatibility with diverse functional groups, simplifying purification and enhancing utility in medicinal chemistry and materials synthesis workflows.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H312-H332
|
|
|
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: