1008-51-1 Usage
Uses
Used in Pharmaceutical Research:
8-Methyl-6-(methylthio)-1H-purine is utilized as a research compound for studying the effects of xanthine derivatives on biological processes. Its stimulant properties, similar to caffeine, make it a valuable tool in understanding the mechanisms of action and potential therapeutic applications of related compounds.
Used in Respiratory Disorder Treatment:
In the pharmaceutical industry, 8-Methyl-6-(methylthio)-1H-purine is used as a potential therapeutic agent for the treatment of asthma and other respiratory disorders. Its ability to modulate biological processes relevant to these conditions positions it as a promising candidate for drug development and treatment strategies.
Used in Food and Beverage Industry:
As a component of caffeine-containing products, 8-Methyl-6-(methylthio)-1H-purine may be found in foods and beverages, contributing to their stimulant effects. Its presence in these products can be relevant for understanding the overall impact of caffeine and its derivatives on consumer health and energy levels.
Check Digit Verification of cas no
The CAS Registry Mumber 1008-51-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,0 and 8 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1008-51:
(6*1)+(5*0)+(4*0)+(3*8)+(2*5)+(1*1)=41
41 % 10 = 1
So 1008-51-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H8N4S/c1-4-10-5-6(11-4)8-3-9-7(5)12-2/h3,5H,1-2H3
1008-51-1Relevant academic research and scientific papers
Mechanisms for the Solvolytic Decompositions of Nucleoside Analogues. IX. Pathways for the Alkyline Hydrolysis of 6-Substituted 9-(1-Ethoxyethyl)purines
Loennberg, Harri,Lehikoinen, Pertti,Neuvonen, Kari
, p. 707 - 712 (2007/10/02)
A few 6-substituted 9-(1-ethoxyethyl)purines have been prepared and the rates of their base-catalyzed hydrolysis were measured by UV spectroscopy.The product mixtures were fractionated by preparative TLC and characterized by NMR and UV spectroscopy.The results obtained suggest that the alkaline cleavage of 9-(1-ethoxyethyl)purines generally proceeds by nucleophilic attack of hydroxide ion on C8 of the purine moiety, resulting in formation of appropriate 4,5-diaminopyrimidine and 8-methylpurine as final products.With 6-methoxy, 6-methylthio, and 6-chloro derivatives nucleophilic attack of hydroxide ion of C6 giving 9-(1-ethoxyethyl)hypoxanthine competes with this reaction.
