Biological activity of various halogenated derivatives of Ioxynil was written by Cooke, A. R.;Hart, R. D.;Achuff, N. E.. And the article was included in Proceedings of the Northeastern Weed Control Conference in 1965.Application of 2314-37-6 This article mentions the following:
Ioxynil (I) is effective for the control of broadleaf weeds and grasses in small grains. The 3,5-dibromo- and 3-bromo- acetates of I and 3,5-dibromo-4-hydroxybenzonitrile acetate are almost as effective. Less active are the 3,5-dichloro, 3-iodo-, 3-bromo-, 3-chloro-, 3,5-dinitro-, and 3-nitro-derivatives of I, p-hydroxybenzonitrile, 3,5-diiodo-4-hydroxybenzamide, 3,5-diiodo-4-hydroxybenzoic acid, 3,5-diiodo-4-hydroxybenzene-sulfonamide, 3,5-diiodo-4-hydroxybenzamide, 3,5-diiodo-4-hydroxybenzaldehyde and its oxime, 3-iodo-p-anisaldehyde, 3,5-dichloro-4-hydroxybenzaldehyde, 3,5-diiodo-4-hydroxyhydrocinnamic acid, p-cyanophenoxyacetic acid, 2,6-dibromo-4-cyanophenoxyacetic acid, 2-chloro-4-cyanophenoxyacetic acid, and 3,-4-diiodosalicylonitrile. In the experiment, the researchers used many compounds, for example, 3-Iodo-4-methoxybenzaldehyde (cas: 2314-37-6Application of 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 of 2314-37-6
Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com