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 175277-67-5
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2,6-Dichloro-4-(trifluoromethyl)pyridin-3-amine features a trifluoromethyl group that enhances electron-withdrawal and metabolic stability, while the dichloro substitution pattern enables selective coupling in late-stage functionalization. This pyridine scaffold serves as a key building block for bioactive heterocycles in medicinal chemistry.
2,6-Dichloro-4-(trifluoromethyl)pyridin-3-amine serves as a versatile building block in medicinal chemistry, enabling efficient access to diverse heterocyclic scaffolds. The dichloro substitution pattern facilitates sequential cross-coupling reactions, while the trifluoromethyl group enhances metabolic stability and lipophilicity. Its amine functionality provides a direct handle for derivatization via amidation, alkylation, or reductive amination, offering high compatibility with standard synthetic workflows. The compound exhibits excellent bench stability and ease of purification, making it well-suited for both exploratory and process-scale applications.
|
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: