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 52351-75-4
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
6-Methoxyindoline-2,3-dione features a methoxy-substituted indoline core with two adjacent carbonyl groups, delivering enhanced solubility and stability compared to unsubstituted analogs. This electron-deficient scaffold integrates readily into synthetic sequences involving nucleophilic addition or cycloaddition reactions, enabling efficient access to complex heterocyclic architectures under standard conditions.
6-Methoxyindoline-2,3-dione serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted indole scaffolds and heterocyclic frameworks. Its methoxy group enhances solubility and modulates reactivity, while the fused diketone system supports diverse transformations including cycloadditions, nucleophilic additions, and transition-metal-catalyzed couplings. Bench-stable and readily purified by recrystallization, it functions reliably in multi-step syntheses for medicinal chemistry and materials applications.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H319
|
|
|
Precautionary Statements : P264-P270-P280-P301+P310-P305+P351+P338-P330-P337+P313-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: