2993-06-8 Usage
Uses
Used in Pharmaceutical Synthesis:
2-(trifluoromethyl)-5H-purin-6-amine serves as a key building block in the creation of various pharmaceuticals. Its unique structure allows it to be a versatile component in the development of new drugs, particularly those targeting specific biological pathways.
Used in Agrochemical Development:
In the agrochemical industry, 2-(trifluoromethyl)-5H-purin-6-amine is utilized for the synthesis of compounds that can address agricultural challenges, such as pest control and crop protection, capitalizing on its ability to interact with biological systems.
Used in Cancer Treatment Research:
2-(trifluoromethyl)-5H-purin-6-amine is explored for its potential role in treating cancer. Its capacity to interact with multiple biological targets suggests that it may have applications in inhibiting cancer cell growth or enhancing the effectiveness of existing cancer therapies.
Used in Medicinal Chemistry Research:
As a valuable tool in medicinal chemistry, 2-(trifluoromethyl)-5H-purin-6-amine aids researchers in understanding the mechanisms of action of various drugs and contributes to the discovery of novel therapeutic agents. Its unique properties make it an important compound for probing and modulating biological activities.
Check Digit Verification of cas no
The CAS Registry Mumber 2993-06-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,9 and 3 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2993-06:
(6*2)+(5*9)+(4*9)+(3*3)+(2*0)+(1*6)=108
108 % 10 = 8
So 2993-06-8 is a valid CAS Registry Number.
2993-06-8Relevant academic research and scientific papers
Preparation method for 2-trifluoromethyl-6-aminopurine
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Paragraph 0023; 0025; 0026; 0029, (2018/09/08)
The invention relates to a preparation method for 2-trifluoromethyl-6-aminopurine. The method comprises the following steps: performing a condensation reaction on 4-formyl-5-aminoimidazole and trifluoroacetamide to obtain a compound 1; performing a chlorination reaction on the compound 1 to obtain a compound 2; performing an ammonolysis reaction on the compound 2 and ammonia in an aminolysis reaction solvent; and after the reaction is completed, performing concentration to dryness, adding a solvent, and performing filtration to obtain the 2-trifluoromethyl-6-aminopurine. The preparation methodprovided by the invention has the advantages that raw materials are cheap and easy to obtain, the synthetic steps are simple, the yield is high, the costs are low and the method is suitable for enlarged production.
