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 77333-45-0
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
4-Bromo-2-methoxy-6-nitroaniline features a nitro group at the para position relative to the amino functionality, enhancing electrophilic reactivity while the methoxy substituent provides electron-donating stabilization. This combination enables selective coupling in cross-coupling reactions and facilitates downstream functionalization in pharmaceutical intermediates and advanced materials synthesis under standard conditions.
4-Bromo-2-methoxy-6-nitroaniline serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling direct incorporation into complex heterocyclic scaffolds via Suzuki-Miyaura and Ullmann coupling reactions. The molecule exhibits robust bench stability, tolerates diverse functional groups, and facilitates efficient purification due to its crystalline nature. Its ortho-substituted arylamine framework supports sequential transformations, making it ideal for the construction of multi-functionalized aromatic systems in lead optimization campaigns.
|
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: