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 4769-96-4
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
6-Nitroindole features a nitro group at the 6-position of the indole scaffold, imparting strong electron-withdrawing character. This functionalization enhances reactivity in transition-metal-catalyzed couplings and facilitates incorporation into bioactive scaffolds. The compound exhibits bench-stable handling properties and serves as a key building block in medicinal chemistry and materials science applications.
6-Nitroindole serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the C6 position via electrophilic substitution or transition-metal-catalyzed coupling. Its electron-deficient indole core enhances reactivity in Pd- and Ni-mediated cross-couplings, while the nitro group facilitates selective reduction to an amine or further derivatization. Bench-stable and readily purified by column chromatography, it functions as a key scaffold for heterocyclic libraries and API intermediates.
|
GHS Pictogram :
|
GHS No : GHS08
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H341
|
|
|
Precautionary Statements : P280-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: