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 182344-23-6
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
4-Fluoro-3-(trifluoromethyl)phenylboronic acid features a fluorinated aryl core with a trifluoromethyl group at the meta position and a boronic acid handle at the para site. This electron-deficient scaffold integrates readily into Suzuki-Miyaura couplings, offering enhanced reactivity and stability under standard conditions. The molecule exhibits improved solubility in polar solvents and maintains bench-stability during handling.
4-Fluoro-3-(trifluoromethyl)phenylboronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl scaffolds. Its trifluoromethyl group enhances metabolic stability and lipophilicity, while the fluorine substituent offers favorable electronic effects and ortho-directing capability. The boronic acid functionality provides excellent bench stability, mild reaction conditions, and compatibility with diverse functional groups, facilitating streamlined synthesis of complex aromatic systems relevant to pharmaceutical and agrochemical development.
|
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: