Quinoline, 2-bromo-8-chloro- is a heterocyclic organic compound characterized by a fused bicyclic structure consisting of a benzene ring and a pyridine ring. This compound features bromine and chlorine substituents at the 2 and 8 positions, respectively, which can influence its reactivity and physical properties. Typically, quinoline derivatives exhibit notable biological activity, making them of interest in medicinal chemistry. The presence of halogen atoms can enhance lipophilicity and alter the compound's interaction with biological targets. Quinoline derivatives are often used as building blocks in the synthesis of pharmaceuticals, agrochemicals, and dyes. The compound's molecular structure contributes to its potential applications in various fields, including organic synthesis and material science. Additionally, its properties such as solubility, melting point, and boiling point can vary based on the specific substituents and their positions on the quinoline ring. As with many halogenated compounds, safety and handling precautions are essential due to potential toxicity and environmental impact.

Quinoline, 2-bromo-8-chloro-

891842-52-7: Quinoline, 2-bromo-8-chloro- is a heterocyclic organic compound characterized by a fused bicyclic structure consisting of a benzene ring and a pyridine ring. This compound features bromine and chlorine substituents at the 2 and 8 positions, respectively, which can influence its reactivity and physical properties. Typically, quinoline derivatives exhibit notable biological activity, making them of interest in medicinal chemistry. The presence of halogen atoms can enhance lipophilicity and alter the compound's interaction with biological targets. Quinoline derivatives are often used as building blocks in the synthesis of pharmaceuticals, agrochemicals, and dyes. The compound's molecular structure contributes to its potential applications in various fields, including organic synthesis and material science. Additionally, its properties such as solubility, melting point, and boiling point can vary based on the specific substituents and their positions on the quinoline ring. As with many halogenated compounds, safety and handling precautions are essential due to potential toxicity and environmental impact.

CAS 891842-52-7

Quinoline, 2-bromo-8-chloro-

Quinoline, 2-bromo-8-chloro-

Ref: IN-DA005OE8

2-Bromo-8-chloroquinoline

Ref: 54-OR93870

2-Bromo-8-chloroquinoline

Ref: 10-F215892

CAS 891842-52-7

Quinoline, 2-bromo-8-chloro-

Quinoline, 2-​bromo-​8-​chloro-

Ref: IN-DA005OE8

2-Bromo-8-chloroquinoline

Ref: 54-OR93870

2-Bromo-8-chloroquinoline

Ref: 10-F215892

Quinoline, 2-bromo-8-chloro-