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 872038-32-9
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This boronate ester features a trifluoromethoxy-substituted benzyl group flanked by tetramethyl-substituted dioxaborolane rings, delivering enhanced stability and moisture tolerance. The electron-withdrawing trifluoromethoxy moiety imparts favorable reactivity in Suzuki-Miyaura cross-coupling, enabling efficient C–C bond formation under mild conditions.
4,4,5,5-Tetramethyl-2-(4-(trifluoromethoxy)benzyl)-1,3,2-dioxaborolane serves as a stable, bench-ready boronate building block for Suzuki-Miyaura cross-coupling reactions. Its trifluoromethoxy-substituted benzyl moiety provides enhanced lipophilicity and metabolic stability, facilitating efficient coupling with aryl and heteroaryl halides. The dioxaborolane framework offers excellent functional group tolerance and ease of purification, making it well-suited for iterative synthesis in medicinal chemistry and API 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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: