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 1073129-57-3
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Methyl 2-Chloro-6-(trifluoromethyl)nicotinate is a bench-stable, electron-deficient heterocyclic ester featuring a trifluoromethyl group at the C6 position and a chlorine atom at C2. This combination enhances its utility in cross-coupling reactions and as a building block for bioactive compounds. The ester functionality enables straightforward derivatization under standard conditions.
Methyl 2-chloro-6-(trifluoromethyl)nicotinate serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling direct functionalization at the C-3 position via cross-coupling reactions. The trifluoromethyl group enhances metabolic stability and lipophilicity, while the ester functionality facilitates downstream transformations. Its bench-stable nature and compatibility with palladium-catalyzed coupling protocols make it a practical choice for constructing complex heterocyclic scaffolds and API intermediates.
|
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: