Application In Synthesis of 5-Iodo-2-furaldehyde. The mechanism of aromatic electrophilic substitution of aromatic heterocycles is consistent with that of benzene. Compound: 5-Iodo-2-furaldehyde, is researched, Molecular C5H3IO2, CAS is 2689-65-8, about Evaluation of the reactivity of furan series aldehydes in catalytic acetalation. Author is Zelikman, Z. I.; Pogrebnaya, V. L.; Kul’nevich, V. G..
First order rate constants, k, are given for the formation, at 80°, of acetals between BuOH, trimethylolethane, trimethylolpropane, or pentaerythritol dichloranhydride and furfuraldehyde or 5-methyl-, chloro-, bromo-, iodo-, or nitrofurfuraldehyde. For equimolar reactant ratios, a 1st order relation is obtainable even though the reaction appears to be bimol. in nature. Velocities increase in the order: Me < Cl < Br < I < NO2, and decrease with increasing size and weight of the polyol. In a given solvent, a linear dependence is noted between the k-band in the absorption spectrum of the aldehyde and the rate constant for the reaction with a given alc., indicating that prediction of rate constants may be feasible by this means. There are many compounds similar to this compound(2689-65-8)Application In Synthesis of 5-Iodo-2-furaldehyde. if you want to know more, you can check out my other articles. I hope it will help you，maybe you’ll find some useful information.
Reference:
1,8-Naphthyridine – Wikipedia,
1,8-Naphthyridine | C8H6N2 – PubChem