Explore: Iodobenzenes

Iodobenzene is an aryl iodide and the simplest of the iodobenzenes, consisting of a benzene ring substituted with one iodine atom. Its chemical formula

Iodobenzenes are a group of aryl iodides/halobenzenes consisting of one or more iodine atoms as substituents on a benzene core. They have the formula C6H6–nIn

This reagent was originally prepared by Conrad Willgerodt by reacting iodobenzene with a mixture of acetic acid and peracetic acid: C6H5I + CH3CO3H + CH3CO2H →

Iodobenzene dichloride (PhICl2) is a complex of iodobenzene with chlorine. As a reagent for organic chemistry, it is used as an oxidant and chlorinating

Bromobenzenes Iodobenzenes Halobenzene may also refer to any of the monosubstituted halobenzenes: Fluorobenzene Chlorobenzene Bromobenzene Iodobenzene Astatobenzene

1-Bromo-4-iodobenzene is a mixed aryl halide (aryl bromide and aryl iodide) with the formula BrC6H4I. In one laboratory route to 1-bromo-4-iodobenzene, 4-bromoaniline

Tetraiodobenzenes form a group of iodobenzenes with four iodine atoms as substituents (C6H2I4). By their different arrangement, three constitutional isomers

original reaction by Tsutomu Mizoroki (1971) describes the coupling between iodobenzene and styrene in methanol to form stilbene at 120 °C (autoclave) with potassium

acid, a common reagent for the oxidation of alcohols to aldehydes, and iodobenzene dichloride (PhICl2), used for the selective chlorination of alkenes and

chlorobenzene is less reactive than fluorobenzene. However, bromobenzene and iodobenzene are about the same or a little more reactive than chlorobenzene, because