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 220107-65-3
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This bench-stable arylmethanol features a para-trifluoromethyl group and an ortho-amino substituent, delivering enhanced electron-withdrawing character and improved solubility in polar organic solvents. The functionalized scaffold enables direct incorporation into bioactive heterocycles and serves as a key intermediate for pharmaceutical and agrochemical synthesis under standard conditions.
(2-Amino-5-(trifluoromethyl)phenyl)methanol serves as a valuable building block in medicinal chemistry, enabling the synthesis of heterocyclic scaffolds and bioactive molecules. Its ortho-amino and benzylic alcohol functionalities offer orthogonal reactivity for sequential transformations, including coupling reactions, cyclizations, and derivatization. The trifluoromethyl group enhances metabolic stability and lipophilicity, while the compound exhibits good bench stability and ease of purification—making it well-suited for scalable synthetic workflows in API development.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H315-H320-H335
|
|
|
Precautionary Statements : P261-P280-P302+P352
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: