Some scientific research about 2689-65-8

If you want to learn more about this compound(5-Iodo-2-furaldehyde)Electric Literature of C5H3IO2, you may wish to communicate with the author of the article,or consult the relevant literature related to this compound(2689-65-8).

Hoyle, William; Roberts, Gordon P.; Meth-Cohn, Otto published the article 《Potential antimicrobial furans》. Keywords: furan antibacterial.They researched the compound: 5-Iodo-2-furaldehyde( cas:2689-65-8 ).Electric Literature of C5H3IO2. Aromatic heterocyclic compounds can be divided into two categories: single heterocyclic and fused heterocyclic. In addition, there is a lot of other information about this compound (cas:2689-65-8) here.

Furan derivatives bearing isosteric and isoelec. functional groups in place of a 2-nitro group lacked antibacterial activity, confirming the essential role of the nitro group in activity. Functional groups employed were sulfo, sulfamoyl, carboxyl, methoxycarbonyl, carbamoyl, and cyano. For example, 5-iodo-2-furaldehyde [2689-65-8] reacted with Cu2(CN)2 in DMF to form 5-formyl-2-furonitrile [42061-89-2], which was condensed with semicarbazide [57-56-7], 3-amino-2-oxazolidinone, or 1-aminohydantoin to yield 5-cyano-2-furancarboxaldehyde semicarbazone [42061-90-5], 3-[[(5-cyano-2-furanyl)methylene]amino]-2-oxazolidinone [42978-22-3], and 1-[[(5-cyano-2-furanyl)methylene]amino]-2,4-imidazolidinedione (I) [42061-92-7], resp.

If you want to learn more about this compound(5-Iodo-2-furaldehyde)Electric Literature of C5H3IO2, you may wish to communicate with the author of the article,or consult the relevant literature related to this compound(2689-65-8).

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