New research progress on 1426129-50-1 in 2021. In classical electrochemical theory, both the electron transfer rate and the adsorption of reactants at the electrode control the electrochemical reaction. 1426129-50-1, Name is (R)-tert-Butyl (1-([1,1′-biphenyl]-4-yl)-3-hydroxypropan-2-yl)carbamate, molecular formurla is C20H25NO3. In a document, author is Liu, Guotao, introducing its new discovery. SDS of cas: 1426129-50-1.
Two naphthalimide-based fluorescent probes containing a thiomorpholine (Np-NS) or a sulfoxide-morpholine (Np-NSO) component are reported. The morpholine unit of non-fluorescent Np-NS and Np-NSO can transform into sulphone-morpholine and be accompanied by blue fluorescence upon oxidative stress, ascribed to the formation of sulphone-morpholine on probes. This sensing behavior displays that they can selectively respond to glutathione to generate a green emission by a sulfonamide-based detection moiety both in vitro and in living cells. Interestingly, the different oxidation states of a sulphur atom on a thiomorpholine ring can be utilized to regulate responsiveness of these probes towards glutathione. Such an oxidation strategy would provide a possibility for enhancing the response rate.
Keep reading other articles of 1426129-50-1. Don’t worry, you don’t need a PhD in chemistry to understand the explanations! SDS of cas: 1426129-50-1.
Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem