1500-85-2 Usage
Uses
Used in Pharmaceutical Synthesis:
4-Amino-7H-pyrrolo[2,3-d]pyrimidine serves as a valuable building block in the synthesis of a wide range of pharmaceuticals and bioactive compounds. Its versatile reactivity allows for the creation of diverse molecular structures with potential therapeutic effects.
Used in Enzyme Inhibition:
4-Amino-7H-pyrrolo[2,3-d]pyrimidine has been investigated for its potential role as an inhibitor of certain enzymes, which could be beneficial in the development of drugs targeting specific enzymatic pathways involved in various diseases.
Used in Organic Electronics:
Due to its semiconducting properties, 4-Amino-7H-pyrrolo[2,3-d]pyrimidine has been studied for its potential use in the field of organic electronics. Its unique electronic characteristics make it a promising candidate for applications in organic semiconductor devices, such as organic light-emitting diodes (OLEDs) and organic field-effect transistors (OFETs).
Check Digit Verification of cas no
The CAS Registry Mumber 1500-85-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,0 and 0 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1500-85:
(6*1)+(5*5)+(4*0)+(3*0)+(2*8)+(1*5)=52
52 % 10 = 2
So 1500-85-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H6N4/c7-5-4-1-2-8-6(4)10-3-9-5/h1-3H,(H3,7,8,9,10)
1500-85-2Relevant academic research and scientific papers
Method for synthesizing 4 -chloropyrropyrimidine compound (by machine translation)
-
, (2020/08/09)
The invention relates to a synthesis method of 4 -lopyrrolopyrimidine compound, which comprises the following steps: mixing 4 -hydroxypyrrolopyrimidine, phosphorus oxychloride and organic base in a temperature range &at;timetimewise and removing excess ethanol to obtain 3 - 7-amino-4 -iodopyrrolopyrimidine; thirdly, dissolving the product 4 -amino-4 -methyl pyrrolopyrimidine in DMF at room temperature and then drying and concentrating 4 -aminopyrrolopyridine. 4 -aminopyrimidine is dissolved in dichloromethane and then subjected to a heat preservation reaction to get -5 -aminopyrrolopyrimidine; and the mixture is dried to remove the solid insoluble matter and is dried and concentrated to yield 12 hours-aminopyrroyrimidine after the heat preservation reaction is carried out; and the solvent is evaporated to remove the solid insoluble matter and is dried and concentrated to remove the solid insoluble matter 4 -5 -7. (by machine translation)
