Benzene, 1-iodo-2-(phenylmethoxy)-, also known by its CAS number 142523-69-1, is an organic compound characterized by the presence of an iodine atom and a phenylmethoxy group attached to a benzene ring. This compound features a benzene core, which is a stable aromatic structure known for its delocalized π-electrons, contributing to its chemical stability and unique reactivity. The iodine substituent can influence the compound's reactivity, particularly in nucleophilic substitution reactions, while the phenylmethoxy group enhances its solubility in organic solvents and may affect its electronic properties. The presence of both iodine and the methoxy group can also impact the compound's physical properties, such as boiling and melting points, as well as its potential applications in organic synthesis and medicinal chemistry. Overall, this compound exemplifies the diverse reactivity and functionalization possibilities within aromatic chemistry.

Benzene, 1-iodo-2-(phenylmethoxy)-

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Benzyloxyiodobenzene is a molecule that can be synthesized in two different ways. One method uses the reaction of benzyl alcohol with iodine and potassium iodide, while the other uses the catellani reaction involving acetone, methyl iodide, sodium hydroxide, and pivalic acid. The yields for both methods are similar. Benzyloxyiodobenzene is an arylated compound that has been shown to catalyze certain chemical reactions. It is also activated by oxygen atoms in the molecule and has been shown to participate in the Catellani reaction with alkyl halides.

CAS 142523-69-1: Benzene, 1-iodo-2-(phenylmethoxy)-

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