Arotsky, Judah’s team published research in Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999) in 1973 | CAS: 41252-95-3

1-Chloro-4-iodo-2-nitrobenzene(cas: 41252-95-3) belongs to organic iodides. Generally organic iodides can be divided into two classes of alkyl iodides and aryl iodides. Application of 41252-95-3 Typical reactions of alkyl iodides include nucleophilic substitution, elimination, reduction, and the formation of organometallics.

The author of 《Iodination and iodo compounds. IV. Effect of substituents and solvent composition on the rate of aromatic iodination by the triiodine cation》 were Arotsky, Judah; Darby, A. Carl; Hamilton, John B. A.. And the article was published in Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999) in 1973. Application of 41252-95-3 The author mentioned the following in the article:

The rate and products of the reaction of deactivated substituted benzenes (e.g., 4-ClC6H4CO2h) and I3+ in H2SO4 were studied. The rate constants were correlated by the electrophilic substituent constants σ+ to give the reaction constant ρ = -6.4. The kinetic isotope effect for the iodination of benzoic acid was kH/kD = 2. The rate of iodination increased as the proportion of H2O in the solvent increased. The results came from multiple reactions, including the reaction of 1-Chloro-4-iodo-2-nitrobenzene(cas: 41252-95-3Application of 41252-95-3)

1-Chloro-4-iodo-2-nitrobenzene(cas: 41252-95-3) belongs to organic iodides. Generally organic iodides can be divided into two classes of alkyl iodides and aryl iodides. Application of 41252-95-3 Typical reactions of alkyl iodides include nucleophilic substitution, elimination, reduction, and the formation of organometallics.

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