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 468060-28-8
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
tert-Butyl (E)-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)allyl)carbamate delivers a bench-stable, moisture-tolerant boronate handle with defined E-geometry. This allylboronate integrates seamlessly into cross-coupling reactions, enabling efficient construction of complex alkenyl architectures under standard conditions. The protecting group remains intact during catalytic transformations, simplifying purification and enhancing functional group compatibility.
tert-Butyl (E)-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)allyl)carbamate serves as a stable, bench-ready allylboron building block for palladium-catalyzed cross-coupling reactions. Its E-configured vinyl boronate enables stereoselective C–C bond formation with aryl and vinyl halides, while the tert-butyl carbamate group provides excellent functional group tolerance and facilitates purification. This reagent is particularly valuable in the synthesis of complex alkenes and heterocyclic scaffolds within medicinal chemistry and process development 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: