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 15540-90-6
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
4,7-Dimethylindoline-2,3-dione is a sterically hindered, bench-stable diketopiperazine derivative featuring electron-deficient aromatic cores. This compound integrates readily into synthetic sequences requiring robust heterocyclic scaffolds under standard conditions. Its methyl substitution pattern enhances solubility and stability in polar aprotic solvents, enabling efficient incorporation into complex molecular architectures.
4,7-Dimethylindoline-2,3-dione serves as a versatile building block in heterocyclic synthesis, enabling efficient access to substituted indole and isoindolinone scaffolds. Its electron-deficient quinone core facilitates Diels-Alder reactions and nucleophilic additions, while the methyl groups enhance solubility and stability under standard reaction conditions. The compound exhibits excellent functional group tolerance and is readily purified by flash chromatography, making it well-suited for iterative synthesis workflows in medicinal chemistry and process development.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H319-H413
|
|
|
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: