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 133046-46-5
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Ethyl 2-(trifluoromethyl)thiazole-4-carboxylate is a bench-stable, moisture-tolerant building block featuring a trifluoromethyl group that imparts strong electron-withdrawing character. This thiazole scaffold integrates readily into pharmaceutical intermediates and agrochemicals, where enhanced metabolic stability and lipophilicity are critical. The ester functionality enables straightforward derivatization under standard conditions.
Ethyl 2-(trifluoromethyl)thiazole-4-carboxylate serves as a versatile building block in medicinal chemistry and synthetic organic chemistry, enabling efficient access to trifluoromethyl-substituted heterocycles. The molecule exhibits excellent bench stability and functional group tolerance, facilitating diverse transformations including nucleophilic substitution, palladium-catalyzed coupling reactions, and cyclization processes. Its electron-deficient thiazole core enhances reactivity in cross-coupling and conjugate addition protocols, making it a practical scaffold for the construction of bioactive molecules and advanced intermediates 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: