Bardot, Valerie et al. published their research in Synlett in 1996 | CAS: 2314-37-6

3-Iodo-4-methoxybenzaldehyde (cas: 2314-37-6) belongs to iodide derivatives. Iodide-containing intermediates are common in organic synthesis, because of the easy formation and cleavage of the C–I bond. Polyiodoorganic compounds are sometimes employed as X-ray contrast agents, in fluoroscopy, a type of medical imaging. This application exploits the X-ray absorbing ability of the heavy iodine nucleus.Application In Synthesis of 3-Iodo-4-methoxybenzaldehyde

A facile synthesis of 2-(2-hydroxyethyl)allylsilanes was written by Bardot, Valerie;Remuson, Roland;Gelas-Mialhe, Yvonne;Gramain, Jean-Claude. And the article was included in Synlett in 1996.Application In Synthesis of 3-Iodo-4-methoxybenzaldehyde This article mentions the following:

Indium-mediated allylsilylation of carbonyl compounds provides a facile and efficient route to 2-(2-hydroxyethyl)allylsilanes. For example, 3-iodo-2-(trimethylsilylmethyl)-1-propene reacts with 2,6-dichlorobenzaldehyde in the presence of In powder in DMF to give 90% 2,6-Cl2C6H3CH(OH)CH2C(:CH2)CH2SiMe3. In the experiment, the researchers used many compounds, for example, 3-Iodo-4-methoxybenzaldehyde (cas: 2314-37-6Application In Synthesis of 3-Iodo-4-methoxybenzaldehyde).

3-Iodo-4-methoxybenzaldehyde (cas: 2314-37-6) belongs to iodide derivatives. Iodide-containing intermediates are common in organic synthesis, because of the easy formation and cleavage of the C–I bond. Polyiodoorganic compounds are sometimes employed as X-ray contrast agents, in fluoroscopy, a type of medical imaging. This application exploits the X-ray absorbing ability of the heavy iodine nucleus.Application In Synthesis of 3-Iodo-4-methoxybenzaldehyde

Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com