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 182344-16-7
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
4-Fluoro-2-(trifluoromethyl)benzeneboronic acid features a strategically positioned trifluoromethyl group and fluorine substituent, enhancing electronic effects and metabolic stability. This electron-deficient boronic acid integrates efficiently into Suzuki-Miyaura cross-coupling reactions under standard conditions, delivering high-yielding access to complex aryl architectures with improved functional group tolerance.
4-Fluoro-2-(trifluoromethyl)benzeneboronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl architectures. The trifluoromethyl group enhances metabolic stability and lipophilicity, while the fluorine substituent facilitates downstream functionalization via nucleophilic aromatic substitution. Its bench-stable boronic acid functionality offers excellent compatibility with diverse reaction conditions and simplifies purification through crystallization or chromatography.
|
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: