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 1279863-38-5
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Ethyl 3-iodo-1H-indazole-5-carboxylate features a strategically positioned iodine atom at the 3-position, enabling efficient late-stage functionalization via cross-coupling reactions. The indazole core provides robust heterocyclic stability, while the ester group offers synthetic versatility for further derivatization. This compound serves as a key intermediate in medicinal chemistry campaigns targeting kinase inhibitors and bioactive nitrogen heterocycles.
Ethyl 3-iodo-1H-indazole-5-carboxylate serves as a versatile building block for constructing indazole-based scaffolds in medicinal chemistry. The iodine substituent enables palladium-catalyzed cross-coupling reactions, including Suzuki, Stille, and Negishi couplings, facilitating rapid diversification of the indazole core. The ester group provides a handle for selective derivatization, while the molecule exhibits good bench stability and ease of purification, making it well-suited for iterative synthesis campaigns and API precursor 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: