CAS 847727-21-3
:8-CHLORO-3-IODOQUINOLINE
Description:
8-Chloro-3-iodoquinoline is a heterocyclic organic compound characterized by its quinoline structure, which consists of a fused benzene and pyridine ring. The presence of chlorine and iodine substituents at the 8 and 3 positions, respectively, significantly influences its chemical properties and reactivity. This compound typically exhibits a pale yellow to brownish appearance and is soluble in organic solvents. It may possess biological activity, making it of interest in medicinal chemistry and pharmaceutical research. The halogen substituents can enhance its potential as a ligand in coordination chemistry or as a precursor in various synthetic pathways. Additionally, the compound's structure suggests potential applications in the development of agrochemicals or as an intermediate in the synthesis of more complex molecules. Safety data should be consulted, as halogenated compounds can exhibit toxicity and environmental persistence. Overall, 8-chloro-3-iodoquinoline is a valuable compound in both research and industrial applications, warranting further investigation into its properties and uses.
Formula:C9H5ClIN
Synonyms:- 8-CHLORO-3-IODOQUINOLINE
- Quinoline, 8-chloro-3-iodo-
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Found 4 products.
8-Chloro-3-iodoquinoline
CAS:Formula:C9H5ClINPurity:97%Color and Shape:SolidMolecular weight:289.50028-Chloro-3-iodoquinoline
CAS:<p>8-Chloro-3-iodoquinoline</p>Purity:97%Molecular weight:289.50017g/mol8-Chloro-3-iodoquinoline
CAS:<p>8-Chloro-3-iodoquinoline is a functionalized aromatic ring that is used in coupling reactions with aryl halides, such as bromides and iodides. Palladium-catalyzed coupling reactions are often more selective than those catalyzed by copper. 8-Chloro-3-iodoquinoline has been shown to be selectively coupled to bromide, which can be used for the synthesis of aryl bromides.</p>Formula:C9H5ClINPurity:Min. 95%Molecular weight:289.5 g/mol
