30066-93-4

Upstream product

• 82138-06-5 5-(2-benzothiazolyl hydrazono)-1,3-dimethylbarbituric acid 

Downstream Products

• 7501-78-2 9-butyl-1,3-dimethyl-8-thio-uric acid 
• 86516-86-1 2,4-diphenyl-7,9-dimethyl-6,8-dioxo-2,3-dihydropyrimidino<5,6-b>-1,5-oxazepine 
• 21544-73-0 5,5-dichloro-1,3-dimethyl-2,4,6(1H,3H,5H)-pyrimidinetrione 
• 2757-85-9 1,3-dimethylalloxan 
• 5429-33-4 5,7-dimethyl-2-phenyloxazolo<5,4-d>pyrimidine-4,6(5H,7H)-dione 
• 79-14-1 glycolic Acid 
• 1216851-27-2 C₁₂H₁₃N₅O₆*H₃N 

Relevant academic research and scientific papers

Electrochemical Behaviour of some Benzothiazolyl-hydrazonobarbituric Acids and Effect of Substituents on Redox-Mechanism

Polarographic and cyclic voltammetric behaviour of twelve titled compounds have been studied in the pH range 2.0-11.2 at dropping mercury electrode, pyrolytic graphite electrode and platinum electrode.The effect of substituents, covering wide range of Hammett substituents constant values, has been evaluated quantitatively.

Electrochemical behaviour of 5-(2-benzothiazolyl hydrazono)-1,3-dimethylbarbituric acid

The electrochemical oxidation and reduction behaviour of 5-(2-benzothiazolyl hydrazono)-1,3-dimethyl barbituric acid has been studied in the pH range 3.0-11.0 at PGE and dropping mercury electrode.The electrochemical oxidation of hydrazones has not previously been studied in detail.The studies reported on hydrazones earlier deal with their reduction.The mechanisms of electrooxidation and electroreduction are suggested on the basis of spectral studies, coulometry and product identification.