On May 18, 2021, Soete, Matthieu; Mertens, Chiel; Aksakal, Resat; Badi, Nezha; Du Prez, Filip published an article.Recommanded Product: 3-Aminodihydrothiophen-2(3H)-one hydrochloride The title of the article was Sequence-Encoded Macromolecules with Increased Data Storage Capacity through a Thiol-Epoxy Reaction. And the article contained the following:
Sequence-encoded oligo(thioether urethane)s with two different coding monomers per backbone unit were prepared via a solid phase, two-step iterative protocol based on thiolactone chem. The first step of the synthetic cycle consists of the thiolactone ring opening with a primary amine, whereby the in situ released thiol is immediately reacted with an epoxide. In the second step, the thiolactone group is reinstalled to initiate the next cycle. This strategy allows to introduce two different coding monomers per synthetic cycle, rendering the resulting macromols. especially attractive in the area of (macro)mol. data storage because of their increased data storage capacity. Subsequently, the efficiency of the herein reported synthesis route and the applicability of the dual-encoded sequence-defined macromols. as a potential data storage platform were demonstrated by unraveling the exact monomer order using tandem mass spectrometry techniques. The experimental process involved the reaction of 3-Aminodihydrothiophen-2(3H)-one hydrochloride(cas: 6038-19-3).Recommanded Product: 3-Aminodihydrothiophen-2(3H)-one hydrochloride
The Article related to sequence encoded macromol data storage thiol epoxy reaction, Chemistry of Synthetic High Polymers: Ring-Opening and Other Polymerizations and other aspects.Recommanded Product: 3-Aminodihydrothiophen-2(3H)-one hydrochloride
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics