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 161798-03-4
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Ethyl 2-(3-formyl-4-isobutoxyphenyl)-4-methylthiazole-5-carboxylate features a formyl group at the meta position relative to a strategically placed isobutoxy substituent, enabling selective functionalization. The thiazole core integrates electron-rich and sterically shielded elements, enhancing stability under standard bench conditions. This scaffold supports modular derivatization in medicinal chemistry workflows.
Ethyl 2-(3-formyl-4-isobutoxyphenyl)-4-methylthiazole-5-carboxylate serves as a versatile building block for the synthesis of functionalized heterocycles and bioactive scaffolds. The pendant aldehyde group enables efficient derivatization via imine formation, reductive amination, or Wittig-type reactions, while the thiazole core provides structural rigidity and potential for metal coordination. The isobutoxy substituent enhances solubility and modulates electronic properties, and the ester functionality supports further transformations such as hydrolysis or cross-coupling. This compound exhibits good bench stability and facilitates straightforward purification by column chromatography, making it well-suited for iterative synthetic campaigns in medicinal chemistry and process 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: