Bakherad, Mohammad’s team published research in Tetrahedron Letters in 2008 | CAS: 41252-95-3

1-Chloro-4-iodo-2-nitrobenzene(cas: 41252-95-3) belongs to organic iodides. The carbon-iodine bond is weaker than other carbon-halogen bonds due to the poor electronegative nature of the iodine atom. Name: 1-Chloro-4-iodo-2-nitrobenzene Organic iodides can be alkyl, alkenyl, or alkynyl, and all of them are very reactive toward with many kinds of nucleophiles.

Name: 1-Chloro-4-iodo-2-nitrobenzeneOn October 20, 2008 ,《Synthesis of 2-benzylimidazo[2,1-b][1,3]benzothiazoles through palladium-catalyzed heteroannulation of acetylenic compounds》 was published in Tetrahedron Letters. The article was written by Bakherad, Mohammad; Nasr-Isfahani, Hossein; Keivanloo, Ali; Sang, Golnaz. The article contains the following contents:

Reactions of 2-imino-3-(2-propynyl)-1,3-benzothiazole with electron-deficient iodobenzenes RI (R = 2-O2NC6H4, 3-O2NC6H4, 4-O2NC6H4, 2-Me-4-O2NC6H3, 2-O2N-4-ClC6H3, 2-Cl-4-O2NC6H3, 3-O2N-4-ClC6H3, 4-NCC6H4, 4-MeO2CC6H4) in the presence of bis(triphenylphosphine)palladium dichloride leads to 2-benzylimidazo[2,1-b][1,3]benzothiazoles I in 55-87% yields. The results came from multiple reactions, including the reaction of 1-Chloro-4-iodo-2-nitrobenzene(cas: 41252-95-3Name: 1-Chloro-4-iodo-2-nitrobenzene)

1-Chloro-4-iodo-2-nitrobenzene(cas: 41252-95-3) belongs to organic iodides. The carbon-iodine bond is weaker than other carbon-halogen bonds due to the poor electronegative nature of the iodine atom. Name: 1-Chloro-4-iodo-2-nitrobenzene Organic iodides can be alkyl, alkenyl, or alkynyl, and all of them are very reactive toward with many kinds of nucleophiles.

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