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 879275-72-6
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This boronate reagent features a difluoromethyl-substituted phenyl group coupled with a stable tetramethyl-1,3,2-dioxaborolane ring. It enables efficient Suzuki-Miyaura couplings under mild conditions, delivering high yields in C–C bond formation. The fluorinated aryl moiety enhances metabolic stability and modulates electronic properties. This bench-stable compound integrates readily into complex molecule synthesis workflows.
This boronate ester serves as a versatile building block in palladium-catalyzed cross-coupling reactions, enabling efficient C–C bond formation with aryl and heteroaryl halides. The difluoromethylphenyl moiety provides enhanced metabolic stability and modulates electronic properties, while the tetramethyl-substituted dioxaborolane ensures excellent bench stability, ease of handling, and compatibility with standard Suzuki-Miyaura conditions. Its robust functional group tolerance facilitates integration into complex molecular architectures common in medicinal chemistry and materials science.
|
GHS Pictogram :
|
GHS No : GHS05,GHS07
|
|
Signal Word : Danger
|
UN#: 1760
|
|
Class : 8
|
Packing Group : Ⅲ
|
|
Hazard Statements : H315-H318-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: