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 1228631-54-6
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This trifluoromethyl-substituted pyridine alcohol features a bench-stable, moisture-tolerant scaffold ideal for late-stage functionalization. The para-trifluoromethyl group imparts strong electron-withdrawing character, while the pendant hydroxyl enables direct derivatization or coupling reactions under standard conditions.
1-(6-(Trifluoromethyl)pyridin-3-yl)ethan-1-ol serves as a valuable building block in medicinal chemistry, enabling direct introduction of a trifluoromethyl-substituted pyridine moiety into target molecules. The alcohol functionality facilitates derivatization via esterification, etherification, or oxidation to the corresponding aldehyde or carboxylic acid. Its bench-stable nature and compatibility with standard coupling protocols make it well-suited for iterative synthesis 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-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: