Chemical Research Letters, May 2021. Redox catalysis has been broadly utilized in electrochemical synthesis. The appropriate choice of redox mediator can avoid electrode passivation, which strongly inhibit the efficient activation of substrates. 103-47-9, Name is N-Cyclohexyltaurine, molecular formula is C8H17NO3S. In an article, author is Hassan, Alaa A.,once mentioned of 103-47-9, Application of 103-47-9.
A Facile Synthesis ofOxoindenothiazine and Dioxospiro(indene-2,4 ‘-thiazine) Derivatives from (Substituted ethylidene)hydrazinecarbothioamides
(E)-2-[2-(1-Substituted ethylidene)hydrazinyl]-5-oxo-9b-hydroxy-5,9b-dihydroindeno[1,2-d][1,3]-thiazine-4-carbonitriles and (E)-5-oxo-[(E)-(1-substituted ethylidene)hydrazinyl]-2,5-dihydroindeno[1,2-d][1,3] thiazine-4-carbonitriles have been obtained from the reaction of 2-(substituted ethylidene)hydrazine-carbothioamides with 2-(1,3-dioxo-2,3-dihydro-1H-inden-2-ylidene) propanedinitrile (1) in ethyl acetate solution. However, (Z)-6′-amino-1,3-dioxo-3′-substituted-2′-[(E)-(1-phenylethylidene) hydrazono]-1,2′, 3,3′-tetrahydrospiro(indene-2,4′-[1,3]thiazine)-5’-carbonitriles were observed during the reaction of N-substituted-2-(1-phenylethylidene)hydrazinecarbothioamides with (1). The structure assignment of products has been confirmed on the basis of H-1-, C-13-NMR, and mass spectrometry, as well as theoretical calculations.
Application of 103-47-9, Because enzymes can increase reaction rates by enormous factors and tend to be very specific, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about 103-47-9.
Reference:
Thiazine – an overview | ScienceDirect Topics,
,Thiazine | C4H5NS – PubChem