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 1507976-00-2
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
6-Chloro-5-iodoindolin-2-one features a sterically constrained indolinone core with complementary halogen substituents enabling selective cross-coupling. The chlorine and iodine atoms facilitate sequential functionalization, while the lactam carbonyl enhances solubility and reactivity in transition-metal-catalyzed transformations under standard conditions.
6-Chloro-5-iodoindolin-2-one serves as a versatile building block for the synthesis of substituted indoles and heterocyclic scaffolds. The ortho-halogenated structure enables palladium-catalyzed cross-coupling reactions, facilitating efficient C–C bond formation under standard conditions. Its bench-stable nature and compatibility with diverse functional groups make it well-suited for iterative synthesis in medicinal chemistry and process development workflows.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H317
|
|
|
Precautionary Statements : P261-P264-P270-P272-P280-P302+P352-P330-P362+P364-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: