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 25724-79-2
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2,3-Dihydro-1-oxo-1H-indene-5-carbonitrile features a fused bicyclic core with a ketone and nitrile group in close proximity, enabling strategic participation in cycloaddition and nucleophilic addition reactions. The electron-deficient indenone scaffold facilitates conjugate additions, while the carbonitrile group serves as a handle for further functionalization under mild conditions. Bench-stable and moisture-tolerant, this compound integrates efficiently into synthetic sequences requiring precise stereocontrol.
2,3-Dihydro-1-oxo-1H-indene-5-carbonitrile serves as a versatile building block in medicinal chemistry, enabling efficient access to substituted indenone scaffolds. Its conjugated enone and nitrile functionalities facilitate nucleophilic additions, Michael reactions, and cyclization cascades under mild conditions. Bench-stable and readily purified by recrystallization, it functions effectively in multistep syntheses requiring orthogonal reactivity and functional group tolerance.
|
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: