The effect of the change of synthetic route on the product 2689-65-8

When you point to this article, it is believed that you are also very interested in this compound(2689-65-8)Safety of 5-Iodo-2-furaldehyde and due to space limitations, I can only present the most important information.

The chemical properties of alicyclic heterocycles are similar to those of the corresponding chain compounds. Compound: 5-Iodo-2-furaldehyde, is researched, Molecular C5H3IO2, CAS is 2689-65-8, about Synthesis and spectral properties of 2-(5-R-2-furylmethylene)-3-oxobutanenitriles, the main research direction is furylmethyleneoxobutanenitrile; butanenitrile furylmethylene; condensation furaldehyde aminobutenenitrile; substituent effect conjugation furylethylene system; LFER furylmethyleneoxobutanenitrile; structure property furylmethyleneoxobutanenitrile.Safety of 5-Iodo-2-furaldehyde.

Substituted 2-(5-R-2-furylmethylene)-3-oxobutanenitriles I (R = H, halo, Ph, etc.) were obtained by condensation of the corresponding 5-R-2-furaldehydes II with 3-amino-2-butenenitrile in acid medium. Relation between the structure and spectral properties (NMR, IR, UV, MS) is presented and the influence of substituents in position 5 of the furan ring on the conjugated 2-furylethylene system is discussed.

When you point to this article, it is believed that you are also very interested in this compound(2689-65-8)Safety of 5-Iodo-2-furaldehyde and due to space limitations, I can only present the most important information.

Reference:
1,8-Naphthyridine – Wikipedia,
1,8-Naphthyridine | C8H6N2 – PubChem