13020-83-2 Usage
Uses
Used in Biochemical Research:
Trimethyl(purin-6-yl)ammonium chloride is used as a biochemical agent for research purposes due to its distinctive purine-based structure, which may facilitate studies in various biological processes and interactions.
Used in Therapeutic Applications:
Trimethyl(purin-6-yl)ammonium chloride is used as a potential therapeutic agent, given its unique properties that could be harnessed for the development of new treatments. However, further research is required to explore its full potential and effects in this area.
Used in Drug Development:
In the pharmaceutical industry, trimethyl(purin-6-yl)ammonium chloride is used as a starting material or intermediate in the synthesis of various drugs, leveraging its chemical reactivity and structural features to create novel therapeutic compounds.
Used in Diagnostic Tools:
Trimethyl(purin-6-yl)ammonium chloride may be utilized in the development of diagnostic tools, such as sensors or imaging agents, due to its chemical and optical properties that could be exploited for detecting or monitoring biological processes.
Note: The specific applications mentioned above are hypothetical and provided as examples based on the general properties of trimethyl(purin-6-yl)ammonium chloride. Actual uses may vary and require further research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 13020-83-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,2 and 0 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 13020-83:
(7*1)+(6*3)+(5*0)+(4*2)+(3*0)+(2*8)+(1*3)=52
52 % 10 = 2
So 13020-83-2 is a valid CAS Registry Number.
13020-83-2Relevant academic research and scientific papers
Deng, Mei,Wang, Ningyu,Xiang, Guangming,Yu, Luoting
, p. 2999 - 3006 (2012)
6-Fluoropurine and its 7-/9-unsubstituted analogues have good biological activity and serve as important pharmaceutical intermediates. This paper describes a new and convenient synthesis of 6-fluoropurine and its 7-/9-unsubstituted analogues, by first replacing the chlorine atoms with trimethylammonio groups through the reaction of 6-chloropurine and its 7-/9-unsubstituted analogues with trimethylamine, and then replacing the trimethylammonio groups with fluorine atoms using safe and cheap TBAF·3H2O as fluorinating agent at room temperature. Compared with reported methods, the new synthesis has milder conditions, shorter reaction times, simpler post-processing and higher (or similar) yields.
