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 187804-79-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This boronic acid features a trifluoromethoxy group that enhances stability and modulates electronic properties, while the fluorinated aryl ring improves metabolic resistance. It integrates readily into Suzuki-Miyaura cross-coupling reactions under standard conditions, delivering high yields with minimal byproduct formation.
(3-Fluoro-4-(trifluoromethoxy)phenyl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl scaffolds. Its stability under ambient conditions and compatibility with diverse functional groups facilitate reliable synthesis of fluorinated aromatic compounds. The trifluoromethoxy moiety enhances metabolic stability and lipophilicity, making it valuable for medicinal chemistry applications.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H315-H319-H335
|
|
|
Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: