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 161395-97-7
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This boronate ester features a (E)-configured allyl acetate handle, enabling efficient palladium-catalyzed cross-coupling under standard conditions. The tetramethyl-substituted dioxaborolane ring imparts exceptional stability and moisture tolerance, while the allyl group facilitates direct incorporation into complex molecular architectures via C–C bond formation.
(E)-3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)allyl acetate serves as a versatile boron-containing building block for palladium-catalyzed cross-coupling reactions. Its terminal olefin functionality enables efficient Suzuki-Miyaura coupling with aryl and vinyl halides, while the acetyl group provides bench stability and facilitates selective deprotection. The tetramethylboronate moiety offers excellent functional group tolerance and compatibility with diverse reaction conditions, making it ideal for constructing complex molecular architectures in medicinal chemistry and materials synthesis.
|
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: