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 1236141-95-9
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Bromo-6-(trifluoromethyl)benzaldehyde features a sterically hindered trifluoromethyl group and an electrophilic aldehyde, enabling direct functionalization in cross-coupling and condensation reactions. The bromine substituent facilitates palladium-catalyzed transformations, while the electron-deficient aromatic ring enhances reactivity in nucleophilic additions. This compound serves as a key building block for pharmaceutical intermediates and advanced materials.
2-Bromo-6-(trifluoromethyl)benzaldehyde serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling palladium-catalyzed cross-coupling reactions due to its ortho-brominated aryl halide functionality. The trifluoromethyl group enhances metabolic stability and lipophilicity, while the aldehyde handles readily participate in reductive amination and condensation reactions. Bench-stable and compatible with diverse functional groups, it facilitates efficient access to complex heterocyclic scaffolds and drug-like molecules.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302
|
|
|
Precautionary Statements : P264-P270-P330-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: