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 919103-45-0
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
6-Iodo-2,3-dihydro-1H-indol-2-one features a iodinated indolinone core with enhanced reactivity at the C6 position, enabling direct functionalization in cross-coupling processes. The lactam moiety provides structural rigidity and polarity, while the iodo substituent facilitates palladium-catalyzed transformations under standard conditions. This compound serves as a key intermediate for bioactive heterocycles in medicinal chemistry.
6-Iodo-2,3-dihydro-1H-indol-2-one serves as a versatile building block for the synthesis of biologically active indole derivatives. Its iodine substituent enables facile palladium-catalyzed cross-coupling reactions, facilitating the construction of complex heterocyclic scaffolds. The dihydroindolinone core provides a stable, bench-compatible platform with predictable reactivity in standard synthetic workflows, supporting efficient functionalization and downstream derivatization.
|
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: