Hart, David J. et al. published their research in Journal of Organic Chemistry in 1985 | CAS: 2314-37-6

3-Iodo-4-methoxybenzaldehyde (cas: 2314-37-6) belongs to iodide derivatives. In general, organic iodides are light-sensitive and turn yellow during storage, owing to the formation of iodine. Iodo alkanes participate in a variety of organic synthesis reactions, which include the Simmons–Smith reaction (cyclopropanation using iodomethane), Williamson ether synthesis, Wittig reaction, Grignard reaction, alkyl coupling reactions, and Wurtz reaction.Recommanded Product: 2314-37-6

Lythraceae alkaloids: total synthesis of (±)-lythrancepine II was written by Hart, David J.;Hong, Won Pyo. And the article was included in Journal of Organic Chemistry in 1985.Recommanded Product: 2314-37-6 This article mentions the following:

A stereoselective total synthesis of the quinolizidine metacyclophane Lythraceae alkaloid lythrancepine-II (I) is described. The quinolizidine nucleus was constructed using an N-acyliminium ion cyclization of amide II. The C(6) sidechain was then introduced and the macrocycle constructed by an intramol. biaryl coupling. The synthesis requires 17 steps and proceeds in approx. 1% overall yield. In the experiment, the researchers used many compounds, for example, 3-Iodo-4-methoxybenzaldehyde (cas: 2314-37-6Recommanded Product: 2314-37-6).

3-Iodo-4-methoxybenzaldehyde (cas: 2314-37-6) belongs to iodide derivatives. In general, organic iodides are light-sensitive and turn yellow during storage, owing to the formation of iodine. Iodo alkanes participate in a variety of organic synthesis reactions, which include the Simmons–Smith reaction (cyclopropanation using iodomethane), Williamson ether synthesis, Wittig reaction, Grignard reaction, alkyl coupling reactions, and Wurtz reaction.Recommanded Product: 2314-37-6

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