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 5350-50-5
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
7-Chloro-3-nitroquinolin-4-ol features a rigid quinoline core bearing a chloro substituent at C7 and a nitro group at C3, creating a strongly electron-deficient scaffold. This configuration enhances its utility in transition-metal-catalyzed cross-coupling reactions and as a building block for bioactive heterocycles. The phenolic hydroxyl at C4 enables direct functionalization or metal chelation.
7-Chloro-3-nitroquinolin-4-ol serves as a versatile building block for the synthesis of quinoline-based pharmaceutical intermediates. Its electron-deficient core enables efficient nucleophilic substitution and transition-metal-catalyzed coupling reactions. The nitro group facilitates selective reduction and further functionalization, while the chloro and hydroxyl substituents offer orthogonal reactivity for scaffold diversification. This compound exhibits good bench stability and is amenable to standard purification protocols, making it well-suited for iterative synthetic campaigns in medicinal chemistry and process development.
|
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: