CAS 69875-54-3
:3-Quinolinecarbonitrile, 2,4-dichloro-
Description:
3-Quinolinecarbonitrile, 2,4-dichloro- is an organic compound characterized by its quinoline structure, which is a bicyclic aromatic compound containing a nitrogen atom in the heterocyclic ring. The presence of a cyano group (-C≡N) at the 3-position and two chlorine substituents at the 2 and 4 positions of the quinoline ring significantly influences its chemical properties. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. It is known for its potential applications in pharmaceuticals and agrochemicals due to its biological activity. The chlorine atoms can enhance the compound's reactivity and influence its interaction with biological targets. Additionally, 3-Quinolinecarbonitrile, 2,4-dichloro- may undergo various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions, making it a valuable intermediate in synthetic organic chemistry. Safety data should be consulted, as halogenated compounds can pose environmental and health risks.
Formula:C10H4Cl2N2
Synonyms:- 3-Cyano-2,4-dichloroquinoline
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Found 4 products.
3-Quinolinecarbonitrile, 2,4-dichloro-
CAS:Formula:C10H4Cl2N2Purity:%Color and Shape:SolidMolecular weight:223.05822,4-Dichloroquinoline-3-carbonitrile
CAS:2,4-Dichloroquinoline-3-carbonitrilePurity:95%Molecular weight:223.06g/mol2,4-Dichloroquinoline-3-carbonitrile
CAS:<p>2,4-Dichloroquinoline-3-carbonitrile is a nitrosourea compound that inhibits cancer cells. It is activated by the addition of a reducing agent such as triethyl orthoformate and then reacts with an amine to form the corresponding N,N'-dichloroquinoline. The product of this reaction inhibits cancer cells by binding to DNA and inhibiting RNA synthesis. 2,4-Dichloroquinoline-3-carbonitrile has been shown to be effective against leukemia cells in vitro.</p>Formula:C10H4Cl2N2Purity:Min. 95%Molecular weight:223.06 g/mol



