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 19689-88-4
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Methoxy-6-nitrobenzaldehyde features a nitro group positioned ortho to the aldehyde, enhancing electrophilicity for efficient coupling reactions. The methoxy substituent provides electron-donating character and improved solubility in organic solvents. This combination enables selective functionalization in synthetic routes requiring activated aromatic aldehydes.
2-Methoxy-6-nitrobenzaldehyde serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted heterocycles and functionalized aromatic scaffolds. Its ortho-directed reactivity, combined with the complementary electronic effects of the methoxy and nitro groups, facilitates regioselective transformations. The aldehyde functionality supports standard condensation reactions, while the nitro group allows for controlled reduction or further functionalization. Bench-stable and readily purified by recrystallization, it functions effectively in multistep syntheses requiring precise substitution patterns.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H312-H332
|
|
|
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P363
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: