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 4295-04-9
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
4-Chloro-6-methoxyquinoline is a heterocyclic compound featuring a quinoline core with strategically positioned electron-withdrawing chlorine and electron-donating methoxy groups. This combination enhances its utility in transition metal-catalyzed cross-coupling reactions, where the substituents modulate reactivity and selectivity. The molecule exhibits good stability under standard conditions and serves as a key building block in medicinal chemistry and materials science applications.
4-Chloro-6-methoxyquinoline serves as a versatile building block in medicinal chemistry and materials science, enabling palladium-catalyzed cross-coupling reactions due to its reactive chloro substituent. The methoxy group enhances solubility and modulates electronic properties, while the quinoline core provides structural rigidity and π-conjugation. This compound exhibits excellent bench stability and facilitates straightforward purification, making it well-suited for iterative synthesis of heterocyclic scaffolds and functionalized aromatic systems.
|
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: