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 157735-10-9
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This boronate ester features a pent-4-en-1-yl group that enables efficient coupling in palladium-catalyzed reactions. The tetramethyl substitution enhances stability and shelf life, while the vinyl handle facilitates further functionalization. Ideal for iterative synthesis workflows requiring robust, moisture-tolerant building blocks.
4,4,5,5-Tetramethyl-2-(pent-4-en-1-yl)-1,3,2-dioxaborolane serves as a stable, bench-ready boron reagent that enables efficient Suzuki-Miyaura cross-coupling reactions. Its sterically protected boronate moiety offers enhanced air and moisture stability, facilitating straightforward handling and purification. The pendant pentenyl group provides a versatile handle for further functionalization, enabling the construction of complex molecular architectures 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-H315-H319-H335
|
|
|
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: