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 123572-65-6
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
4-Fluoro-1-nitro-2-(trifluoromethoxy)benzene features a trifluoromethoxy group flanked by electron-withdrawing nitro and fluoro substituents, creating a highly electron-deficient aromatic core. This configuration enables efficient coupling in cross-coupling reactions and facilitates nucleophilic substitution under mild conditions. The compound exhibits bench-stable handling characteristics and demonstrates compatibility with diverse reaction environments.
4-Fluoro-1-nitro-2-(trifluoromethoxy)benzene serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its ortho-fluoro and nitro functionalities. The trifluoromethoxy group enhances metabolic stability and lipophilicity, while the nitro group provides a handle for reduction to an amine or further functionalization. Bench-stable and compatible with standard synthetic workflows, it facilitates efficient construction of complex heterocyclic scaffolds and API intermediates.
|
GHS Pictogram :
|
GHS No : GHS06
|
|
Signal Word : Danger
|
UN#: 2810
|
|
Class : 6.1
|
Packing Group : Ⅲ
|
|
Hazard Statements : H301-H311-H331
|
|
|
Precautionary Statements : P261-P264-P270-P271-P280-P285-P302+P352-P304+P340-P330-P361-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: