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 364-12-5
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
5-Bromo-2-iodobenzotrifluoride delivers a dual halogen handle for cross-coupling, combining a bromine at the meta position with an iodine at the ortho site relative to the trifluoromethyl group. This arrangement enables sequential functionalization under orthogonal reaction conditions. The molecule exhibits enhanced stability and solubility in common organic solvents, facilitating handling in synthetic workflows.
5-Bromo-2-iodobenzotrifluoride serves as a versatile dihalogenated building block for palladium-catalyzed cross-coupling reactions. The ortho-bromo and iodo substituents enable sequential functionalization, while the trifluoromethyl group imparts enhanced metabolic stability and lipophilicity—key attributes in medicinal chemistry scaffolds. Bench-stable and compatible with standard coupling protocols, it facilitates efficient access to complex fluorinated biaryls and heterocycles.
|
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: