Most of the compounds have physiologically active properties, and their biological properties are often attributed to the heteroatoms contained in their molecules, and most of these heteroatoms also appear in cyclic structures. A Journal, Zhurnal Organicheskoi Khimii called Kinetics and mechanism of the acetalation of 5-substituted furfural, Author is Kul’nevich, V. G.; Zelikman, Z. I.; Pustovarov, V. S., which mentions a compound: 2689-65-8, SMILESS is IC1=CC=C(O1)C=O, Molecular C5H3IO2, Application In Synthesis of 5-Iodo-2-furaldehyde.
The rate of formation of acetals from 5-substituted furfurals (I, R = Er2N, Me2N, Me, H, Cl, Br, I, NO2) and pentaerythritol dichlorohydrin, MeC(CH2OH)3, EtC(CH2OH)3, or BuOH in C6H6 in the presence of KU-2 cation-exchange resin (H form) increased in the stated order of R and alcs. The rate constants correlated with the Brown σn+ constants of R.
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Reference:
1,8-Naphthyridine – Wikipedia,
1,8-Naphthyridine | C8H6N2 – PubChem