3-Fluoroisoquinoline is a heterocyclic aromatic compound characterized by the presence of a fluorine atom at the 3-position of the isoquinoline ring system. Its molecular structure consists of a fused benzene and pyridine ring, contributing to its aromaticity and stability. The presence of the fluorine atom introduces unique electronic properties, influencing the compound's reactivity and potential applications in medicinal chemistry and material science. 3-Fluoroisoquinoline is typically a colorless to pale yellow liquid or solid, depending on its form, and exhibits moderate solubility in organic solvents. It is known for its role as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. The compound's reactivity can be attributed to the electron-withdrawing nature of the fluorine atom, which can affect nucleophilic substitution reactions. Additionally, 3-fluoroisoquinoline may exhibit biological activity, making it a subject of interest in drug discovery and development. Safety data should be consulted for handling and storage, as with all chemical substances.

3-fluoroisoquinoline

396-29-2: 3-Fluoroisoquinoline is a heterocyclic aromatic compound characterized by the presence of a fluorine atom at the 3-position of the isoquinoline ring system. Its molecular structure consists of a fused benzene and pyridine ring, contributing to its aromaticity and stability. The presence of the fluorine atom introduces unique electronic properties, influencing the compound's reactivity and potential applications in medicinal chemistry and material science. 3-Fluoroisoquinoline is typically a colorless to pale yellow liquid or solid, depending on its form, and exhibits moderate solubility in organic solvents. It is known for its role as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. The compound's reactivity can be attributed to the electron-withdrawing nature of the fluorine atom, which can affect nucleophilic substitution reactions. Additionally, 3-fluoroisoquinoline may exhibit biological activity, making it a subject of interest in drug discovery and development. Safety data should be consulted for handling and storage, as with all chemical substances.

CAS 396-29-2

3-fluoroisoquinoline

3-Fluoroisoquinoline

Ref: IN-DA00CIUD

3-Fluoroisoquinoline

Ref: 54-PC535070

3-Fluoroisoquinoline

Ref: 10-F335081