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 497959-33-8
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Bromo-4-(trifluoromethyl)benzyl alcohol features a brominated aromatic ring paired with a trifluoromethyl group, delivering enhanced electron-withdrawing character and improved metabolic stability. The pendant hydroxyl group enables direct functionalization or derivatization in synthetic workflows. This compound serves as a valuable intermediate in the development of bioactive molecules and advanced materials.
2-Bromo-4-(trifluoromethyl)benzyl alcohol serves as a versatile building block in medicinal chemistry and materials synthesis. The bromo group enables palladium-catalyzed cross-coupling reactions, while the benzylic alcohol facilitates derivatization via oxidation or protection. Its trifluoromethyl moiety imparts enhanced metabolic stability and lipophilicity, making it valuable for constructing bioactive scaffolds. The compound exhibits good bench stability and is amenable to standard purification techniques.
|
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: