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 190788-59-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This boronate ester features a nitro-substituted aryl group and tetramethyl substitution, delivering enhanced stability and reactivity in Suzuki-Miyaura coupling. The electron-deficient nitrophenyl moiety enables efficient cross-coupling under standard conditions, while the dioxaborolane scaffold ensures bench-stable handling and minimal protodeboronation.
4,4,5,5-Tetramethyl-2-(2-nitrophenyl)-1,3,2-dioxaborolane serves as a stable, bench-ready boron reagent enabling efficient Suzuki-Miyaura cross-coupling reactions. Its ortho-nitroaryl group facilitates directed metalation and enhances regioselectivity in heterocyclic synthesis. The tetramethyl-substituted dioxaborolane core ensures excellent air and moisture stability, simplifying handling and purification. Functions reliably in diverse reaction conditions, supporting scalable synthesis of complex biaryls and functionalized aromatic scaffolds.
|
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: