CAS 128676-94-8
:3-Quinolinol, 2-chloro-
Description:
3-Quinolinol, 2-chloro- is a chemical compound characterized by its quinoline structure, which consists of a fused benzene and pyridine ring. The presence of a hydroxyl group (-OH) at the 3-position and a chlorine atom at the 2-position contributes to its unique properties. This compound is typically a pale yellow to brown solid and is soluble in organic solvents. It exhibits potential biological activity, making it of interest in medicinal chemistry and pharmacology. The chlorine substituent can influence its reactivity and interaction with biological targets. Additionally, 3-Quinolinol, 2-chloro- may participate in various chemical reactions, such as nucleophilic substitutions or electrophilic aromatic substitutions, due to the electron-withdrawing nature of the chlorine atom. Safety data indicates that, like many chlorinated compounds, it should be handled with care due to potential toxicity and environmental concerns. Overall, this compound serves as a valuable intermediate in organic synthesis and may have applications in developing pharmaceuticals or agrochemicals.
Formula:C9H6ClNO
Synonyms:- 2-Chloro-3-hydroxyquinoline
- 2-Chloroquinolin-3-Ol
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Found 3 products.
2-Chloroquinolin-3-ol
CAS:Formula:C9H6ClNOPurity:95.0%Color and Shape:Liquid, No data available.Molecular weight:179.62-Chloroquinolin-3-ol
CAS:<p>2-Chloroquinolin-3-ol is an orally active, organic solvent-free, synthetic drug that is a basic compound. It has been shown to have anti-inflammatory properties and can be used for the treatment of inflammatory diseases such as rheumatoid arthritis. The drug has also been shown to be effective against autoimmune diseases such as type 1 diabetes mellitus. 2-Chloroquinolin-3-ol is an analogue of quinolinic acid, which is found in plants and animals. 2CQOL binds to chloride channels on the surface of cells, which prevents the influx of chloride ions into the cell and leads to cytotoxicity.</p>Formula:C9H6ClNOPurity:Min. 95%Molecular weight:179.6 g/mol


