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 1198787-23-3
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This piperidine-2,6-dione scaffold features a 5-nitro-1-oxoisoindoline moiety that imparts strong electron-withdrawing character, enhancing reactivity in conjugate addition and cycloaddition processes. The fused ring system provides rigidity and defined spatial orientation, enabling precise molecular positioning in synthetic intermediates. Bench-stable under standard conditions, it integrates readily into complex heterocyclic architectures.
3-(5-Nitro-1-oxoisoindolin-2-yl)piperidine-2,6-dione serves as a versatile scaffold for constructing bioactive heterocycles, leveraging the electron-deficient isoindolinone core and flanking diketone functionality. The nitro group enhances electrophilicity for nucleophilic addition, while the piperidinedione moiety provides a rigid, polar framework suitable for metal-catalyzed coupling and solid-phase synthesis. This compound enables efficient access to complex polycyclic systems under standard bench conditions, exhibiting robust stability and compatibility with common functional groups.
|
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-P330-P362+P364-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: