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 263149-10-6
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
4-Chloro-7-hydroxy-6-methoxyquinoline-3-carbonitrile features a polar quinoline core with strategically positioned electron-withdrawing nitrile and chloro groups, enabling robust conjugation and enhanced reactivity in transition metal-catalyzed couplings. The hydroxy and methoxy substituents provide solubility and hydrogen-bonding capacity, supporting its use in medicinal chemistry and fluorescent probe development under standard conditions.
4-Chloro-7-hydroxy-6-methoxyquinoline-3-carbonitrile serves as a versatile heterocyclic building block for medicinal chemistry and materials science applications. Its combination of hydroxyl, methoxy, cyano, and chloro substituents enables selective functionalization via cross-coupling, nucleophilic substitution, and derivatization reactions. The molecule exhibits good bench stability and facilitates efficient purification, making it well-suited for iterative synthesis workflows targeting complex quinoline-based scaffolds.
|
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: