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 2216750-84-2
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This quinolinone derivative features a methylated amino group and a pendant acetamide moiety, enabling integration into bioactive scaffolds. The electron-rich dihydroquinoline core supports conjugation in medicinal chemistry applications, while the ether linkage enhances metabolic stability under standard conditions.
2-((6-Amino-1-methyl-2-oxo-1,2-dihydroquinolin-3-yl)oxy)-N-methylacetamide serves as a versatile intermediate in the synthesis of quinoline-based medicinal scaffolds. Its amino and amide functionalities enable selective derivatization, while the dihydroquinoline core provides structural rigidity and compatibility with standard coupling reactions. Bench-stable and readily purified by chromatography, it facilitates efficient access to functionalized heterocycles relevant to drug discovery programs.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H312-H332
|
|
|
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: