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 406232-79-9
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
4-Bromo-1-chloro-2-(trifluoromethoxy)benzene features a trifluoromethoxy group that enhances electron-withdrawal and metabolic stability, while the bromo and chloro substituents enable selective cross-coupling reactions. This aryl halide integrates readily into complex scaffolds under standard palladium-catalyzed conditions.
4-Bromo-1-chloro-2-(trifluoromethoxy)benzene serves as a versatile building block in cross-coupling chemistry, enabling efficient construction of complex aryl architectures. The orthogonal reactivity of bromo and chloro groups facilitates sequential functionalization, while the trifluoromethoxy substituent provides enhanced metabolic stability and lipophilicity—key attributes in medicinal chemistry. This compound exhibits excellent bench stability and compatibility with standard Pd-catalyzed reactions, simplifying purification and scale-up in API synthesis workflows.
|
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: