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 871126-22-6
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This boronic acid features a fluorinated aryl scaffold with a formyl group positioned ortho to the boronic acid moiety, enabling selective coupling in Suzuki-Miyaura reactions. The electron-withdrawing fluorine enhances reactivity while maintaining bench stability, and the formyl functionality allows for downstream derivatization via condensation or reduction.
(2-Fluoro-4-formylphenyl)boronic acid serves as a versatile building block in transition-metal-catalyzed cross-coupling reactions, enabling efficient construction of biaryl and heteroaryl architectures. The ortho-fluoro substituent enhances regioselectivity in subsequent transformations, while the formyl group provides a handle for derivatization via condensation or reductive amination. Bench-stable and compatible with standard Suzuki-Miyaura coupling conditions, it facilitates rapid access to functionalized aromatic scaffolds relevant to medicinal chemistry and materials science.
|
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: