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 1341125-78-7
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
5-Bromo-3-(trifluoromethyl)benzofuran features a bromine substituent and a trifluoromethyl group positioned ortho to each other on the benzofuran core. This electron-deficient scaffold enables direct functionalization in transition-metal-catalyzed cross-coupling reactions, serving as a key building block for bioactive heterocycles and advanced materials.
5-Bromo-3-(trifluoromethyl)benzofuran serves as a versatile building block in medicinal chemistry and materials science, enabling palladium-catalyzed cross-coupling reactions due to its reactive bromine substituent. The trifluoromethyl group enhances metabolic stability and lipophilicity, while the benzofuran core provides a rigid, planar scaffold suitable for targeted molecular design. Bench-stable and compatible with standard synthetic workflows, it facilitates efficient construction of complex heterocyclic architectures.
|
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-P330-P362+P364-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: