Recently I am researching about MULTIBLOCK COPOLYMERS; BLOCK-COPOLYMER; ENE REACTIONS; MICELLES; TRANSFORMATION; EXCHANGE; POLYSTYRENE; CHEMISTRY; VESICLES; NETWORKS, Saw an article supported by the University of Potsdam. Quality Control of 2,2′-Disulfanediyldiethanamine dihydrochloride. Published in ROYAL SOC CHEMISTRY in CAMBRIDGE ,Authors: Hess, A; Schmidt, BVKJ; Schlaad, H. The CAS is 56-17-7. Through research, I have a further understanding and discovery of 2,2′-Disulfanediyldiethanamine dihydrochloride
A series of polystyrene- and poly(methyl methacrylate)-dithioesters was subjected to aminolysis under ambient atmospheric conditions, i.e., in the presence of oxygen. Polymer disulfide coupling by oxidation occurred within tens of minutes and the yield of disulfide-coupled polymer increased with decreasing polymer molar mass. Oxidation of thiolates is usually an unwanted side reaction, here it is employed to obtain exclusively polymeric mixed disulfides through in situ aminolysis/functionalization in the presence of a thiol. The in situ aminolysis/functionalization in the presence of a disulfide, Ellman’s reagent or polymer disulfide, resulted in the exclusive formation of polymer-dithionitrobenzoic acid, which can be further reacted with a thiol to exchange the terminal functionality, or block copolymer with dynamic disulfide linker, respectively.
Quality Control of 2,2′-Disulfanediyldiethanamine dihydrochloride. Bye, fridends, I hope you can learn more about C4H14Cl2N2S2, If you have any questions, you can browse other blog as well. See you lster.
Reference:
Thiazine – an overview | ScienceDirect Topics,
,Thiazine | C4H5NS – PubChem