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 40107-07-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
4-Chloro-6-iodoquinoline is a halogenated quinoline scaffold featuring complementary reactive sites for cross-coupling. The chlorine and iodine substituents enable sequential functionalization, with the iodo group serving as a high-reactivity handle in palladium-catalyzed transformations. This electron-deficient heterocycle integrates readily into complex molecular architectures under standard conditions.
4-Chloro-6-iodoquinoline serves as a versatile building block in transition-metal-catalyzed cross-coupling reactions, enabling efficient construction of biaryl and heterobiaryl architectures. The orthogonal reactivity of the chloro and iodo substituents allows sequential functionalization under selective conditions. Its bench-stable nature and compatibility with palladium- and nickel-based catalysis make it well-suited for medicinal chemistry and materials synthesis workflows.
|
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: