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 1701435-39-3
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This boronic acid features a benzyloxy group ortho to a trifluoromethyl-substituted phenyl ring, delivering enhanced stability and solubility in polar organic media. The electron-deficient arylboron moiety enables efficient Suzuki-Miyaura coupling under mild conditions, facilitating rapid assembly of complex biaryl architectures in medicinal chemistry and materials synthesis.
(2-(Benzyloxy)-4-(trifluoromethyl)phenyl)boronic acid serves as a versatile building block in Suzuki-Miyaura coupling reactions, enabling efficient C–C bond formation under mild conditions. The trifluoromethyl group imparts enhanced metabolic stability and lipophilicity, while the benzyloxy functionality provides orthogonal protection and improved solubility. Its bench-stable nature and compatibility with diverse functional groups make it ideal for constructing complex aryl scaffolds in medicinal chemistry and materials science applications.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H312-H332
|
|
|
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: