4-Fluoroquinoline is a heterocyclic aromatic compound characterized by a quinoline structure with a fluorine atom substituted at the fourth position. Its molecular formula is C9H6FN, indicating it contains nine carbon atoms, six hydrogen atoms, one fluorine atom, and one nitrogen atom. This compound exhibits a pale yellow to light brown appearance and is known for its aromatic properties, which contribute to its stability and reactivity. 4-Fluoroquinoline is soluble in organic solvents but has limited solubility in water. It is primarily used in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of antimicrobial agents. The presence of the fluorine atom can enhance the biological activity and lipophilicity of the compound, making it a valuable building block in medicinal chemistry. Additionally, 4-Fluoroquinoline can undergo various chemical reactions, including electrophilic substitutions and nucleophilic additions, which are essential for further functionalization in synthetic applications. Safety data should be consulted for handling and exposure risks, as with any chemical substance.

4-Fluoroquinoline

394-70-7: 4-Fluoroquinoline is a heterocyclic aromatic compound characterized by a quinoline structure with a fluorine atom substituted at the fourth position. Its molecular formula is C9H6FN, indicating it contains nine carbon atoms, six hydrogen atoms, one fluorine atom, and one nitrogen atom. This compound exhibits a pale yellow to light brown appearance and is known for its aromatic properties, which contribute to its stability and reactivity. 4-Fluoroquinoline is soluble in organic solvents but has limited solubility in water. It is primarily used in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of antimicrobial agents. The presence of the fluorine atom can enhance the biological activity and lipophilicity of the compound, making it a valuable building block in medicinal chemistry. Additionally, 4-Fluoroquinoline can undergo various chemical reactions, including electrophilic substitutions and nucleophilic additions, which are essential for further functionalization in synthetic applications. Safety data should be consulted for handling and exposure risks, as with any chemical substance.

CAS 394-70-7

4-Fluoroquinoline

4-Fluoroquinoline

Ref: IN-DA00341O

4-Fluoroquinoline

Ref: 54-PC421219

4-Fluoroquinoline

Ref: 10-F618930