Redox catalysis has been broadly utilized in electrochemical synthesis due to its kinetic advantages over direct electrolysis. 154445-78-0, Name is 2,2,4,6,7-Pentamethyl-2,3-dihydrobenzofuran-5-sulfonyl chloride, molecular formula is , belongs to thiazines compound. The appropriate choice of redox mediator can avoid electrode passivation and overpotential.In a document, author is Orlova, M. A., Name: 2,2,4,6,7-Pentamethyl-2,3-dihydrobenzofuran-5-sulfonyl chloride.
The distribution of complexes (ZnLCl2)-Zn-69m-Cl-1, [Zn-69m(L-2)(2)]Cl-2, and [Zn-69m(L-2)(2)]Sal(2) (L-1 is N-(5,6-dihydro-4H-1,3-thiazin-2-yl)benzamide, L-2 is 2-aminopyrimidine, Sal is a salicylate ion) in vivo in mice
The distribution of complexes of thiazine and pyrimidine derivatives possessing antileukemic activity and labeled with radionuclide Zn-69m in the organs of mice and its rate of excretion were studied. A solution of ZnCl2 was used for comparison. An increase in the time of excretion of the drug from the body and a decrease of its penetration into the brain in the presence of a salicylate ion were observed.
I hope this article can help some friends in scientific research. I am very proud of our efforts over the past few months and hope to 154445-78-0 help many people in the next few years. Name: 2,2,4,6,7-Pentamethyl-2,3-dihydrobenzofuran-5-sulfonyl chloride.
Reference:
Thiazine – an overview | ScienceDirect Topics,
,Thiazine | C4H5NS – PubChem