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 1063697-17-5
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-(Trifluoromethyl)pyridin-3-ol features a trifluoromethyl group at the 2-position and a hydroxyl moiety at the 3-position of the pyridine ring, creating a uniquely electron-deficient heteroaromatic scaffold. This configuration enhances its utility in transition metal-catalyzed coupling reactions and as a building block in medicinal chemistry. The molecule exhibits bench-stable handling characteristics and moderate solubility in common organic solvents.
2-(Trifluoromethyl)pyridin-3-ol serves as a versatile building block in medicinal chemistry, enabling efficient access to fluorinated heterocyclic scaffolds. Its trifluoromethyl group enhances metabolic stability and lipophilicity, while the phenolic hydroxyl offers direct functionalization potential. The compound exhibits bench stability and facilitates coupling reactions with aryl halides, sulfonates, and electrophiles under standard catalytic conditions. It functions effectively in Suzuki-Miyaura, Ullmann, and direct arylation protocols, supporting rapid diversification in drug discovery campaigns.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H315-H319
|
|
|
Precautionary Statements : P264-P270-P280-P302+P352-P330-P362+P364-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: