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 328956-60-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This boronic acid features a fluorinated aryl ring paired with a formyl group, enabling selective coupling in Suzuki-Miyaura reactions. The electron-deficient aromatic system enhances reactivity while maintaining bench-stable handling under standard conditions.
(3-Fluoro-5-formylphenyl)boronic acid serves as a versatile building block in Suzuki-Miyaura coupling reactions, enabling the efficient construction of biaryl scaffolds with precise substitution patterns. The formyl group provides orthogonal reactivity for downstream modifications, including oxime formation or reductive amination, while the boronic acid functionality ensures compatibility with aqueous conditions and mild reaction parameters. Bench-stable and readily purified by recrystallization, it facilitates streamlined synthesis of functionalized aromatic systems relevant to medicinal chemistry and materials science.
|
GHS Pictogram :
|
GHS No : GHS05
|
|
Signal Word : Danger
|
UN#: 3261
|
|
Class : 8
|
Packing Group : Ⅲ
|
|
Hazard Statements : H314
|
|
|
Precautionary Statements : P260-P264-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P363-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: