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 1160924-51-5
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
tert-Butyl (E)-4-(2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)vinyl)piperidine-1-carboxylate is a bench-stable boronate ester featuring a conjugated vinylpiperidine scaffold. This building block enables palladium-catalyzed cross-coupling reactions under mild conditions, delivering functionalized piperidine derivatives with high regioselectivity and yield. The tetramethyl-substituted dioxaborolane moiety enhances stability and reactivity in Suzuki-Miyaura processes.
tert-Butyl (E)-4-(2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)vinyl)piperidine-1-carboxylate serves as a versatile boron-containing building block for palladium-catalyzed cross-coupling reactions. The (E)-configured vinylborane moiety enables efficient Suzuki-Miyaura coupling with aryl and heteroaryl halides, while the piperidine scaffold offers a stable, bench-accessible platform for late-stage functionalization. The tert-butyl carbamate group provides excellent stability and facilitates straightforward deprotection under mild acidic conditions, enhancing its utility in complex molecule synthesis.
|
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: