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 10222-62-5
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Methoxyquinoline-4-carboxylic acid features a quinoline core functionalized with a methoxy group at the 2-position and a carboxylic acid at the 4-position, offering enhanced solubility and stability. This combination enables direct integration into medicinal chemistry scaffolds, particularly in kinase inhibitors and bioactive heterocycles, where the electron-donating methoxy group modulates reactivity and binding affinity.
2-Methoxyquinoline-4-carboxylic acid serves as a versatile building block in medicinal chemistry, enabling direct incorporation into bioactive scaffolds via standard coupling reactions. Its ortho-methoxy substitution enhances solubility and modulates electronic properties, while the carboxylic acid group facilitates amide, ester, and heterocycle formation under mild conditions. Bench-stable and readily purified, it functions reliably in parallel synthesis and API development workflows.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302
|
|
|
Precautionary Statements : P264-P270-P330-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: