Pankratov, Alexei N.’s team published research in Afinidad in 2001 | CAS: 41252-95-3

1-Chloro-4-iodo-2-nitrobenzene(cas: 41252-95-3) belongs to organic iodides. Alkyl iodides react at a faster rate than alkyl fluorides due to the weak C-I bond.Application In Synthesis of 1-Chloro-4-iodo-2-nitrobenzeneIodo alkanes participate in a variety of organic synthesis reactions, which include the Simmons–Smith reaction (cyclopropanation using iodomethane), Williamson ether synthesis, Wittig reaction, Grignard reaction, alkyl coupling reactions, and Wurtz reaction.

《Nucleophilic aromatic substitution for benzene derivatives: substituent rate factors from quantum chemical computations》 was written by Pankratov, Alexei N.. Application In Synthesis of 1-Chloro-4-iodo-2-nitrobenzene And the article was included in Afinidad on April 30 ,2001. The article conveys some information:

The anionic localization energies (Λ-) for the reaction of 1-chloro-2-nitro-4-substituted benzenes with the methoxide anion have been computed by the PM3 method. Substituent rate factors correlate linearly with the Λ- values. In the experiment, the researchers used 1-Chloro-4-iodo-2-nitrobenzene(cas: 41252-95-3Application In Synthesis of 1-Chloro-4-iodo-2-nitrobenzene)

1-Chloro-4-iodo-2-nitrobenzene(cas: 41252-95-3) belongs to organic iodides. Alkyl iodides react at a faster rate than alkyl fluorides due to the weak C-I bond.Application In Synthesis of 1-Chloro-4-iodo-2-nitrobenzeneIodo alkanes participate in a variety of organic synthesis reactions, which include the Simmons–Smith reaction (cyclopropanation using iodomethane), Williamson ether synthesis, Wittig reaction, Grignard reaction, alkyl coupling reactions, and Wurtz reaction.

Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com