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 1218790-40-9
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This boronate moiety integrates a trifluoromethylated pyrazole scaffold, enabling efficient cross-coupling under standard conditions. The tetramethyl-dioxaborolane group ensures high stability and compatibility with palladium-catalyzed reactions, delivering robust yields in Suzuki-Miyaura transformations.
4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-3-(trifluoromethyl)-1H-pyrazole serves as a versatile boronate building block in palladium-catalyzed cross-coupling reactions. Its trifluoromethyl group enhances metabolic stability and modulates electronic properties, while the robust dioxaborolane moiety enables reliable coupling under mild conditions. The compound exhibits excellent bench stability, facile purification, and broad functional group tolerance, making it well-suited for constructing complex heterocyclic scaffolds in medicinal chemistry and materials science applications.
|
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: