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 43142-64-9
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Ethyl 7-chloro-1H-indole-2-carboxylate features a chlorinated indole core with a carboxylate ester at the C2 position, offering enhanced electron deficiency and stability. This scaffold integrates readily into synthetic routes targeting biologically active heterocycles, particularly in medicinal chemistry applications requiring robust, moisture-tolerant intermediates.
Ethyl 7-chloro-1H-indole-2-carboxylate serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the C7 position of the indole scaffold. The electron-withdrawing chlorine substituent enhances electrophilicity at C3 and C6, facilitating subsequent cross-coupling reactions. Its ester group allows for controlled hydrolysis or derivatization, supporting access to diverse indole-based intermediates. Bench-stable and readily purified by column chromatography, it functions effectively in standard synthetic workflows involving Pd-catalyzed couplings, nucleophilic substitutions, and heterocycle elaboration.
|
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: