Kamali, Taghi A.’s team published research in Tetrahedron Letters in 2009 | 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.Iodo 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.Related Products of 41252-95-3

Related Products of 41252-95-3On September 30, 2009 ,《Synthesis of 6-substituted imidazo[2,1-b]thiazoles via Pd/Cu-mediated Sonogashira coupling in water》 was published in Tetrahedron Letters. The article was written by Kamali, Taghi A.; Bakherad, Mohammad; Nasrollahzadeh, Mahmoud; Farhangi, Shiva; Habibi, Davood. The article contains the following contents:

The reaction of 2-amino-3-(2-propynyl)thiazolium bromide with various iodobenzenes, catalyzed by Pd/Cu, in the presence of sodium lauryl sulfate as surfactant and Cs2CO3 as base, in water, leads to the formation of 6-substituted imidazo[2,1-b]thiazoles. In the experiment, the researchers used 1-Chloro-4-iodo-2-nitrobenzene(cas: 41252-95-3Related Products of 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.Iodo 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.Related Products of 41252-95-3

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