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 349-56-4
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
3-Methoxy-5-(trifluoromethyl)phenol features a trifluoromethyl group that imparts strong electron-withdrawing character, enhancing reactivity in electrophilic substitution. The methoxy substituent contributes resonance donation, balancing electronic effects. This dual-functionalized phenol offers enhanced stability and solubility in organic media, enabling efficient incorporation into pharmaceutical intermediates and advanced materials synthesis under standard conditions.
3-Methoxy-5-(trifluoromethyl)phenol serves as a versatile building block in medicinal chemistry and agrochemical synthesis, offering a strategically positioned trifluoromethyl group for enhanced metabolic stability and lipophilicity. The phenolic hydroxyl enables direct derivatization via etherification or esterification, while the methoxy and trifluoromethyl substituents provide orthogonal reactivity and favorable electronic modulation. Bench-stable and compatible with standard coupling protocols, it facilitates efficient construction of complex heterocyclic scaffolds and functionalized aromatic systems.
|
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: