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 903130-38-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-(Trifluoromethyl)thiazole-5-carbaldehyde features a trifluoromethyl group that enhances electron-withdrawal and metabolic stability, while the thiazole ring provides a rigid, polar scaffold. The aldehyde functionality enables direct coupling in multistep syntheses, particularly for bioactive heterocycles and pharmaceutical intermediates. This compound exhibits excellent bench-stability and compatibility with standard synthetic protocols.
2-(Trifluoromethyl)thiazole-5-carbaldehyde serves as a versatile building block in medicinal chemistry, enabling the synthesis of heterocyclic scaffolds through standard coupling reactions. Its trifluoromethyl group enhances metabolic stability and lipophilicity, while the aldehyde functionality facilitates efficient derivatization via reductive amination, nucleophilic addition, or condensation reactions. Bench-stable and compatible with common protecting groups, it functions reliably in multi-step synthetic sequences for 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: