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 87240-06-0
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
7-Bromo-5-nitroindoline integrates a bromine substituent and a nitro group at distinct positions on the indoline scaffold, enabling selective functionalization in cross-coupling and electrophilic substitution reactions. The electron-deficient nature of the nitro group enhances reactivity in transition-metal-catalyzed transformations, while the bromo handle facilitates further diversification. This compound exhibits bench-stable handling characteristics under standard conditions, making it suitable for use in synthetic medicinal chemistry and materials development workflows.
7-Bromo-5-nitroindoline serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the indoline core through palladium-catalyzed cross-coupling reactions. The bromo group facilitates C–C bond formation under standard Suzuki, Stille, or Negishi conditions, while the nitro group provides a handle for selective reduction and subsequent derivatization. Its bench-stable nature and compatibility with diverse reaction conditions make it well-suited for iterative synthesis of complex heterocyclic scaffolds.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H315-H319-H320
|
|
|
Precautionary Statements : P264-P280-P302+P352-P338-P362
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: