1500-85-2 Usage
General Description
4-Amino-7H-pyrrolo[2,3-d]pyrimidine is a heterocyclic compound with the chemical formula C6H6N4. It is a pyrrolopyrimidine derivative and has a fused-ring structure composed of a pyrrole ring fused to a pyrimidine ring. 4-Amino-7H-pyrrolo[2,3-d]pyrimidine is commonly used as a building block in the synthesis of various pharmaceuticals and bioactive compounds due to its versatile reactivity. It has also been investigated for its potential biological activities, including its role as an inhibitor of certain enzymes. Additionally, 4-Amino-7H-pyrrolo[2,3-d]pyrimidine has also been studied for its potential use in the field of organic electronics due to its semiconducting properties. Overall, this chemical compound has a wide range of potential uses and applications in various fields of science and technology.
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 articles and documents
Method for synthesizing 4 -chloropyrropyrimidine compound (by machine translation)
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, (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)
