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 5622-34-4
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This quinolinyl-acetic acid derivative integrates a quinolin-6-yl moiety linked to a carboxylic acid group, offering enhanced solubility and metabolic stability. The electron-deficient quinoline ring facilitates conjugation in synthetic transformations, while the pendant acetic acid enables direct derivatization. This structure supports applications in medicinal chemistry and materials science where rigid, planar scaffolds with functional handles are required.
2-(Quinolin-6-yl)acetic acid serves as a versatile building block for medicinal chemistry and materials science, enabling efficient access to quinoline-containing scaffolds. Its carboxylic acid functionality facilitates direct derivatization via amide coupling, esterification, or metal-catalyzed transformations. The molecule exhibits good bench stability and compatibility with common protecting group strategies, making it well-suited for iterative synthesis workflows in API development and heterocyclic library construction.
|
GHS Pictogram :
|
GHS No : GHS06
|
|
Signal Word : Danger
|
UN#: 2811
|
|
Class : 6.1
|
Packing Group : Ⅲ
|
|
Hazard Statements : H301
|
|
|
Precautionary Statements : P264-P270-P330-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: