4-Fluoro-1,2-diiodobenzene is an aromatic compound characterized by the presence of a fluorine atom and two iodine atoms attached to a benzene ring. The fluorine atom is located at the para position relative to the iodine substituents, which are positioned at the ortho positions. This substitution pattern influences the compound's physical and chemical properties, such as its reactivity and polarity. The presence of halogens, particularly iodine, typically enhances the compound's electron-withdrawing characteristics, which can affect its behavior in electrophilic aromatic substitution reactions. Additionally, the bulky iodine atoms can introduce steric hindrance, influencing the compound's reactivity and interactions with other molecules. 4-Fluoro-1,2-diiodobenzene is generally insoluble in water but may dissolve in organic solvents. Its applications may include use in organic synthesis, pharmaceuticals, and materials science, particularly in the development of functionalized aromatic compounds. Safety precautions should be taken when handling this compound, as halogenated compounds can pose health and environmental risks.

4-fluoro-1,2-diiodobenzene

203059-85-2: 4-Fluoro-1,2-diiodobenzene is an aromatic compound characterized by the presence of a fluorine atom and two iodine atoms attached to a benzene ring. The fluorine atom is located at the para position relative to the iodine substituents, which are positioned at the ortho positions. This substitution pattern influences the compound's physical and chemical properties, such as its reactivity and polarity. The presence of halogens, particularly iodine, typically enhances the compound's electron-withdrawing characteristics, which can affect its behavior in electrophilic aromatic substitution reactions. Additionally, the bulky iodine atoms can introduce steric hindrance, influencing the compound's reactivity and interactions with other molecules. 4-Fluoro-1,2-diiodobenzene is generally insoluble in water but may dissolve in organic solvents. Its applications may include use in organic synthesis, pharmaceuticals, and materials science, particularly in the development of functionalized aromatic compounds. Safety precautions should be taken when handling this compound, as halogenated compounds can pose health and environmental risks.

CAS 203059-85-2

4-fluoro-1,2-diiodobenzene

1,2-Diiodo-4-fluorobenzene

Ref: IN-DA00BC1O

1,2-Diiodo-4-fluorobenzene

Ref: 54-PC8196

3,4-Diiodofluorobenzene

Ref: 10-F013307