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 2982-53-8
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Methyl 2-(4,5-dimethoxy-2-nitrophenyl)acetate features a nitro-substituted aromatic core flanked by two methoxy groups, enhancing electron-withdrawing character and stability. The ester functionality enables direct integration into cross-coupling or cyclization sequences under standard conditions. This bench-stable compound serves as a key intermediate in the synthesis of functionalized heterocycles and bioactive scaffolds.
Methyl 2-(4,5-dimethoxy-2-nitrophenyl)acetate serves as a versatile building block for nitroaryl-containing heterocycles and pharmaceutical intermediates. The dimethoxy substitution pattern enhances solubility and stabilizes the nitro group against premature reduction, enabling controlled functionalization. Its ester moiety facilitates subsequent transformations including nucleophilic substitution, hydrogenation, or coupling reactions, while the ortho-nitro group directs electrophilic aromatic substitution. Bench-stable and readily purified by flash chromatography, it functions effectively in multi-step syntheses of bioactive scaffolds.
|
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-P280-P302+P352
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: