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 1006-47-9
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
8-Iodoquinoline delivers a potent iodine substituent at the quinoline scaffold, enabling direct functionalization in cross-coupling reactions. This electron-deficient heterocycle combines enhanced reactivity with bench-stable handling, making it ideal for constructing complex pharmaceutical intermediates and materials precursors under standard conditions.
8-Iodoquinoline serves as a versatile building block in synthetic organic chemistry, enabling palladium-catalyzed cross-coupling reactions due to its well-established reactivity profile. The iodine substituent facilitates efficient C–C and C–heteroatom bond formation under standard conditions, while the quinoline core provides inherent stability and orthogonal functionality for further derivatization. Its bench-stable nature and compatibility with diverse reaction environments make it a practical choice for constructing complex heterocyclic scaffolds in medicinal chemistry and materials science applications.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H315-H319
|
|
|
Precautionary Statements : P264-P280-P302+P352-P305+P351+P338-P332+P313-P337+P313-P362+P364
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: