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 113438-59-8
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Methyl 3-(cyanomethyl)-1H-indole-5-carboxylate features a strategically positioned cyano group at the benzylic position, enhancing electrophilicity for downstream functionalization. The indole core provides a rigid, electron-rich scaffold ideal for bioactive molecule synthesis. This bench-stable derivative integrates seamlessly into pharmaceutical and agrochemical development workflows.
Methyl 3-(cyanomethyl)-1H-indole-5-carboxylate serves as a versatile building block in medicinal chemistry, enabling efficient access to indole-based scaffolds. The cyanomethyl group facilitates subsequent transformations such as hydrolysis, nucleophilic addition, and cyclization, while the methyl ester allows for selective reduction or amidation. Its bench-stable nature and compatibility with standard coupling and functionalization protocols make it ideal for parallel synthesis and API intermediate development.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H312-H332
|
|
|
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P363-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: