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 885520-50-3
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
6-Bromo-4-nitro-1H-indole features a bromine substituent at the 6-position and a nitro group at the 4-position on the indole core, creating a highly electron-deficient heterocycle. This combination enables direct functionalization in cross-coupling reactions and facilitates incorporation into complex molecular architectures requiring precise electronic tuning.
6-Bromo-4-nitro-1H-indole serves as a versatile building block for functionalized indole scaffolds, enabling palladium-catalyzed cross-coupling reactions at the bromine site and nitro group reduction to afford key intermediates in medicinal chemistry. Its stability under standard reaction conditions and compatibility with diverse transformations make it well-suited for synthesis of biologically active heterocycles and API precursors.
|
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-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: