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 387350-39-2
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This pyridine derivative features a strategically positioned aminomethyl group and a trifluoromethyl moiety, enabling robust functionalization in synthetic pathways. The electron-withdrawing trifluoromethyl substituent enhances reactivity at the pyridine ring while maintaining stability under standard conditions. Ideal for coupling reactions and as a building block in medicinal chemistry and agrochemical development.
3-(Aminomethyl)-6-(trifluoromethyl)pyridine serves as a versatile building block in medicinal chemistry, enabling direct access to bioactive heterocyclic scaffolds. The primary amine functionality facilitates conjugation and derivatization, while the trifluoromethyl group enhances metabolic stability and lipophilicity. Its pyridine core supports standard coupling reactions and functional group interconversions, making it suitable for modular synthesis of kinase inhibitors and other targeted therapeutics. The compound exhibits good bench stability and is readily purified by standard chromatographic methods.
|
GHS Pictogram :
|
GHS No : GHS05
|
|
Signal Word : Danger
|
UN#: 2735
|
|
Class : 8
|
Packing Group : Ⅲ
|
|
Hazard Statements : H314
|
|
|
Precautionary Statements : P280-P301+P330+P331-P302+P352-P304+P340
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: