4-Fluoro-3-iodobenzonitrile is an organic compound characterized by the presence of a benzene ring substituted with both a fluorine atom and an iodine atom, as well as a nitrile group (-C≡N). The fluorine atom is located at the para position (4-position) relative to the nitrile group, while the iodine atom is at the meta position (3-position). This compound is typically a solid at room temperature and is known for its potential applications in pharmaceuticals and organic synthesis due to the reactivity of the nitrile group and the presence of halogen substituents, which can influence the compound's electronic properties and reactivity. The presence of both halogens can also affect the compound's polarity and solubility in various solvents. Additionally, 4-fluoro-3-iodobenzonitrile may exhibit interesting chemical behavior in reactions such as nucleophilic substitutions or coupling reactions, making it a valuable intermediate in synthetic organic chemistry. Safety precautions should be taken when handling this compound, as it may pose health risks typical of halogenated organic compounds.

4-fluoro-3-iodobenzonitrile

159719-57-0: Benzonitrile, 4-Fluoro-3-Iodo-, 4-Fluoro-3-iodobenzonitrile

4-Fluoro-3-iodobenzonitrile

4-Fluoro-3-iodobenzonitrile is a deactivated aromatic compound that has been iodinated. The fluorine atom in this molecule is highly reactive and can be used to react with other molecules to form new compounds. 4-Fluoro-3-iodobenzonitrile is not toxic, but its reactions with other chemicals may produce toxic byproducts. This chemical belongs to the group of halogenated aromatic compounds, which are often used as solvents or disinfectants. Bromination of 4-fluoro-3-iodobenzonitrile produces 4-bromo-3,5,6,7,8,9,10-hexahydrobenzo[a]pyrene (BHP), a known carcinogenic agent.

CAS 159719-57-0: 4-fluoro-3-iodobenzonitrile

4-Fluoro-3-iodobenzonitrile

Ref: 54-PC9106

4-Fluoro-3-iodobenzonitrile

Ref: 3D-JGA71957

4-Fluoro-3-iodobenzonitrile

Ref: 10-F050221

Benzonitrile, 4-fluoro-3-iodo-

Ref: IN-DA001RCP