3-Bromo-5-(4-fluorophenyl)pyridine is a heterocyclic organic compound characterized by its pyridine ring, which is substituted at the 3-position with a bromine atom and at the 5-position with a 4-fluorophenyl group. This compound features a pyridine structure, which is a six-membered aromatic ring containing one nitrogen atom, contributing to its basicity and potential reactivity. The presence of the bromine and fluorine substituents enhances its electrophilic properties, making it useful in various chemical reactions, including nucleophilic substitutions and coupling reactions. The fluorine atom can also influence the compound's electronic properties, potentially affecting its solubility and reactivity. 3-Bromo-5-(4-fluorophenyl)pyridine is often utilized in medicinal chemistry and material science, serving as a building block for the synthesis of more complex molecules. Its unique structural features may impart specific biological activities, making it of interest in drug discovery and development. As with many halogenated compounds, it is essential to handle it with care due to potential environmental and health impacts.

3-bromo-5-(4-fluorophenyl)pyridine

675590-04-2: 3-Bromo-5-(4-fluorophenyl)pyridine is a heterocyclic organic compound characterized by its pyridine ring, which is substituted at the 3-position with a bromine atom and at the 5-position with a 4-fluorophenyl group. This compound features a pyridine structure, which is a six-membered aromatic ring containing one nitrogen atom, contributing to its basicity and potential reactivity. The presence of the bromine and fluorine substituents enhances its electrophilic properties, making it useful in various chemical reactions, including nucleophilic substitutions and coupling reactions. The fluorine atom can also influence the compound's electronic properties, potentially affecting its solubility and reactivity. 3-Bromo-5-(4-fluorophenyl)pyridine is often utilized in medicinal chemistry and material science, serving as a building block for the synthesis of more complex molecules. Its unique structural features may impart specific biological activities, making it of interest in drug discovery and development. As with many halogenated compounds, it is essential to handle it with care due to potential environmental and health impacts.

CAS 675590-04-2

3-bromo-5-(4-fluorophenyl)pyridine

3-Bromo-5-(4-fluorophenyl)pyridine

Ref: IN-DA00FAS5

3-Bromo-5-(4-fluorophenyl)pyridine

Ref: 54-PC1007137

3-Bromo-5-(4-fluorophenyl)pyridine

Ref: 10-F067250