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 402-05-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Bromo-5-(trifluoromethyl)phenol features a trifluoromethyl group that imparts enhanced electron-withdrawal and metabolic stability, while the bromo substituent enables facile cross-coupling transformations. This phenolic scaffold integrates readily into pharmaceutical intermediates and functional materials under standard conditions.
2-Bromo-5-(trifluoromethyl)phenol serves as a versatile building block in the synthesis of functionalized aromatic scaffolds, enabling efficient late-stage functionalization via palladium-catalyzed cross-coupling reactions. The bromo group facilitates Suzuki, Stille, and Negishi couplings, while the phenolic hydroxyl offers sites for etherification or esterification. Its trifluoromethyl substituent enhances metabolic stability and lipophilicity, making it valuable in medicinal chemistry and agrochemical development. Bench-stable and readily purified by recrystallization, it integrates seamlessly into standard synthetic workflows.
|
GHS Pictogram :
|
GHS No : GHS05
|
|
Signal Word : Danger
|
UN#: 1759
|
|
Class : 8
|
Packing Group : Ⅲ
|
|
Hazard Statements : H302+H312+H332-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: