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 943310-52-9
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
5-Fluoro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde delivers a boronate-functionalized aryl aldehyde with enhanced stability and moisture tolerance. The electron-deficient benzaldehyde core pairs effectively with palladium catalysts in Suzuki-Miyaura couplings. This bench-stable reagent enables efficient C–C bond formation under standard conditions.
5-Fluoro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde serves as a versatile boronate building block for Suzuki-Miyaura cross-coupling reactions. The aldehyde group enables direct functionalization or derivatization, while the pinacol boronate moiety provides excellent stability, ease of handling, and compatibility with a broad range of coupling partners. Its utility in constructing biaryl and heterocyclic scaffolds makes it a valuable reagent for 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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: