2,8-Dichloroquinoline is an organic compound characterized by its quinoline structure, which consists of a fused benzene and pyridine ring. It features two chlorine substituents located at the 2 and 8 positions of the quinoline ring, which significantly influence its chemical properties and reactivity. This compound is typically a pale yellow to brown solid at room temperature and is sparingly soluble in water but more soluble in organic solvents such as ethanol and acetone. 2,8-Dichloroquinoline exhibits biological activity, making it of interest in medicinal chemistry, particularly for its potential use in pharmaceuticals and agrochemicals. Its chlorine atoms can enhance lipophilicity and alter the compound's interaction with biological targets. Additionally, it may undergo various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions, due to the presence of the electron-rich aromatic system. Safety precautions should be taken when handling this compound, as it may pose health risks, including potential toxicity.

2,8-Dichloroquinoline

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2,8-dichloroquinoline

2,8-Dichloroquinoline is a zerovalent metal compound that has a functional group of chloride. 2,8-Dichloroquinoline reacts with amines to form quinoline derivatives and can be used in labeling amine groups. It has a reactive and fluorescent character that can be used for transfer or labeling purposes. 2,8-Dichloroquinoline is also an effective ligand for transition metals such as nickel, cobalt, and iron. The fluorescence properties of this compound make it ideal for immunofluorescence studies.

CAS 4470-83-1: 2,8-Dichloroquinoline

2,8-dichloroquinoline

Ref: 54-OR901662

2,8-Dichloroquinoline

Ref: IN-DA003G79

2,8-Dichloroquinoline

Ref: 10-F092044

2,8-Dichloroquinoline

Ref: 3D-FD42213