Название продукции:5-(Quinolin-8-ylthio)furan-2-carbaldehyde

IUPAC Name:5-(quinolin-8-ylsulfanyl)furan-2-carbaldehyde

CAS:332018-99-2
Молекулярная формула:C14H9NO2S
Чистота:97%
Номер в каталоге:CM258346
Молекулярная масса:255.29

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Информация о продукции

Номер CAS:332018-99-2
Молекулярная формула:C14H9NO2S
Точка плавления:-
Smiles-код:O=CC1=CC=C(SC2=C3N=CC=CC3=CC=C2)O1
Плотность:
Номер в каталоге:CM258346
Молекулярная масса:255.29
Точка кипения:
Номер Mdl:
Хранение:

Category Infos

Furans
Furan is a cyclic flammable liquid compound C4H4O that is obtained from wood oils of pines or made synthetically and is used especially in organic synthesis. Furan is aromatic because a pair of lone pair electrons of the oxygen atom in its molecule forms a large π bond in the plane of the conjugated orbital, making a total of 6 electrons in the plane of the conjugated plane, conforming to the 4n+2 structure. Aromaticity makes furan have the property of easy substitution and difficult addition. The other lone pair of electrons in oxygen stretches out. The oxygen atom itself conforms to sp2 hybridization. Due to the presence of the aromatic ring, the chemical behavior of furan is not very similar to that of other unsaturated heterocycles. The oxygen in the aromatic ring has an electron-donating effect, so the electrophilic substitution reactivity of furan is stronger than that of benzene.
Furan | C4H4O | Where to Buy Furans-Chemenu
Furane | Furanes | Furfuran | Furan | C4H4O | Furan Synthesis | Where to Buy Furans
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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 5-(Quinolin-8-ylthio)furan-2-carbaldehyde, also known as QTF, is a heterocyclic compound that has been extensively studied for its potential applications in various scientific fields. QTF is a versatile molecule that has shown promising results in the areas of organic synthesis, medicinal chemistry, and material science.
Synthesis and Application The synthesis of 5-(Quinolin-8-ylthio)furan-2-carbaldehyde involves the reaction of 5-acetylfuran-2-carbaldehyde and 8-mercaptoquinoline in the presence of a base. The reaction proceeds via the formation of an intermediate, which is subsequently oxidized to yield 5-(Quinolin-8-ylthio)furan-2-carbaldehyde. This method has been optimized to yield high purity 5-(Quinolin-8-ylthio)furan-2-carbaldehyde in good yields. 5-(Quinolin-8-ylthio)furan-2-carbaldehyde has been extensively studied for its potential applications in various scientific fields. In organic synthesis, 5-(Quinolin-8-ylthio)furan-2-carbaldehyde has been used as a building block for the synthesis of various heterocyclic compounds. In medicinal chemistry, 5-(Quinolin-8-ylthio)furan-2-carbaldehyde has been shown to exhibit potent antitumor activity against a variety of cancer cell lines. In material science, 5-(Quinolin-8-ylthio)furan-2-carbaldehyde has been used as a precursor for the synthesis of luminescent materials.
Future Directions There are many potential future directions for the study of 5-(Quinolin-8-ylthio)furan-2-carbaldehyde. One area of research could be the development of more efficient and cost-effective methods for the synthesis of 5-(Quinolin-8-ylthio)furan-2-carbaldehyde. Another area of research could be the investigation of the mechanism of action of 5-(Quinolin-8-ylthio)furan-2-carbaldehyde and its potential applications in the treatment of various diseases. Additionally, the development of 5-(Quinolin-8-ylthio)furan-2-carbaldehyde-based materials for various applications could be an interesting area of research.