5-Fluoroisoquinoline is a heterocyclic aromatic compound characterized by its isoquinoline structure, which consists of a fused benzene and pyridine ring. The presence of a fluorine atom at the 5-position of the isoquinoline ring significantly influences its chemical properties and reactivity. This compound is typically a pale yellow to brown solid at room temperature and is known for its relatively low solubility in water, but it can dissolve in organic solvents such as ethanol and dichloromethane. 5-Fluoroisoquinoline exhibits interesting biological activities, making it a subject of interest in medicinal chemistry, particularly in the development of pharmaceuticals. Its fluorine substitution can enhance lipophilicity and metabolic stability, which are desirable traits in drug design. Additionally, this compound can participate in various chemical reactions, including electrophilic substitutions and nucleophilic additions, due to the electron-withdrawing nature of the fluorine atom. Overall, 5-Fluoroisoquinoline serves as a valuable building block in organic synthesis and medicinal applications.

5-Fluoroisoquinoline

394-66-1: 5-Fluoroisoquinoline is a heterocyclic aromatic compound characterized by its isoquinoline structure, which consists of a fused benzene and pyridine ring. The presence of a fluorine atom at the 5-position of the isoquinoline ring significantly influences its chemical properties and reactivity. This compound is typically a pale yellow to brown solid at room temperature and is known for its relatively low solubility in water, but it can dissolve in organic solvents such as ethanol and dichloromethane. 5-Fluoroisoquinoline exhibits interesting biological activities, making it a subject of interest in medicinal chemistry, particularly in the development of pharmaceuticals. Its fluorine substitution can enhance lipophilicity and metabolic stability, which are desirable traits in drug design. Additionally, this compound can participate in various chemical reactions, including electrophilic substitutions and nucleophilic additions, due to the electron-withdrawing nature of the fluorine atom. Overall, 5-Fluoroisoquinoline serves as a valuable building block in organic synthesis and medicinal applications.

CAS 394-66-1

5-Fluoroisoquinoline

5-Fluoroisoquinoline

Ref: IN-DA00CK52

5-Fluoroisoquinoline

Ref: 54-PC107754

5-Fluoro-isoquinoline

Ref: 3D-AAA39466