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 56136-84-6
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This acetyl derivative features a 6-nitrobenzo[d][1,3]dioxole scaffold, delivering enhanced stability and solubility in organic media. The electron-deficient nitro group facilitates electrophilic functionalization, while the ketone moiety enables direct coupling or reduction pathways. Ideal for synthesizing bioactive heterocycles under standard bench conditions.
1-(6-Nitrobenzo[d][1,3]dioxol-5-yl)ethan-1-one serves as a versatile synthetic building block for nitro-substituted heterocycles, enabling efficient access to bioactive scaffolds via standard electrophilic and nucleophilic transformations. The ketone functionality offers reliable site-specific derivatization, while the ortho-nitro group enhances reactivity in coupling and cyclization reactions. Bench-stable and amenable to purification by recrystallization or flash chromatography, it functions effectively in multi-step syntheses targeting pharmaceutical intermediates and functional materials.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H315-H319
|
|
|
Precautionary Statements : P264-P270-P280-P302+P352-P330-P362+P364-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: