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 16382-17-5
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Ethyl 5-ethoxy-1H-indole-2-carboxylate features a bench-stable indole core with a strategically positioned ethoxy group at the 5-position, enhancing solubility and reactivity. The ester functionality enables straightforward derivatization, facilitating access to diverse indole-based scaffolds in medicinal chemistry and materials science applications.
Ethyl 5-ethoxy-1H-indole-2-carboxylate serves as a versatile building block for indole-based heterocycles, enabling efficient access to substituted indoles via hydrolysis, decarboxylation, or cross-coupling reactions. The ethoxy group at the C5 position enhances solubility and stability, while the ester functionality supports diverse transformations under standard conditions. Its bench-stable nature and compatibility with palladium-catalyzed coupling protocols make it ideal for medicinal chemistry and process development workflows.
|
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-P280-P302+P352
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: