Product Name:N1-(8-quinolyl)-2-chloroacetamide

IUPAC Name:2-chloro-N-(quinolin-8-yl)acetamide

CAS:32889-11-5
Molecular Formula:C11H9ClN2O
Purity:97%
Catalog Number:CM224866
Molecular Weight:220.66

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Product Details

CAS NO:32889-11-5
Molecular Formula:C11H9ClN2O
Melting Point:-
Smiles Code:O=C(NC1=C2N=CC=CC2=CC=C1)CCl
Density:
Catalog Number:CM224866
Molecular Weight:220.66
Boiling Point:
MDL No:
Storage:

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Quinolines
Quinolines are an important class of biologically active heterocyclic compounds, and their derivatives usually exhibit a variety of biological activities. They can be used as antimalarial drugs and in the preparation of other antimalarial drugs. Other important activities of quinoline derivatives include inhibitory activity against EGFR-TK and antipsychotic activity. Futhermore, quinoline scaffolds are present in various drug molecules, including the antimalarial drugs aablaquine, chloroquine, mefloquine and primaquine, and the antibacterial agents gatifloxacin, levofloxacin, and moxifloxacin.
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Product Overview N1-(8-quinolyl)-2-chloroacetamide, also known as CQ, is a chemical compound that has been extensively studied for its potential use in scientific research. CQ is a member of the quinoline family of compounds and has been found to have a range of biochemical and physiological effects.
Synthesis and Application The synthesis of N1-(8-quinolyl)-2-chloroacetamide involves the reaction of 8-hydroxyquinoline with chloroacetyl chloride in the presence of a base. The resulting product is then purified by recrystallization. This synthesis method has been well documented in the scientific literature and has been used to produce N1-(8-quinolyl)-2-chloroacetamide for use in research studies. N1-(8-quinolyl)-2-chloroacetamide has been extensively studied for its potential use in scientific research. One of the main areas of research has been its use as a fluorescent probe for the detection of metal ions. N1-(8-quinolyl)-2-chloroacetamide has been found to bind to a range of metal ions, including zinc, copper, and iron, and can be used to detect changes in metal ion concentrations in biological systems. In addition to its use as a fluorescent probe, N1-(8-quinolyl)-2-chloroacetamide has also been studied for its potential anti-cancer properties. Studies have shown that N1-(8-quinolyl)-2-chloroacetamide can induce apoptosis, or programmed cell death, in cancer cells. This has led to interest in using N1-(8-quinolyl)-2-chloroacetamide as a potential cancer therapy.
Future Directions There are several future directions for research on N1-(8-quinolyl)-2-chloroacetamide. One area of interest is its potential use as a cancer therapy. Further studies are needed to determine the optimal dosage and delivery method for N1-(8-quinolyl)-2-chloroacetamide, as well as its potential side effects. Another area of interest is the development of new fluorescent probes based on the structure of N1-(8-quinolyl)-2-chloroacetamide. These probes could be used to detect a wider range of metal ions and could have potential applications in the diagnosis and treatment of diseases. Overall, N1-(8-quinolyl)-2-chloroacetamide is a promising compound with a range of potential applications in scientific research. Further studies are needed to fully understand its mechanism of action and potential uses.