128850-53-3 Usage
Pyrimidine derivative
The compound belongs to the group of pyrimidine derivatives, which are known for their importance in biological systems and potential applications in medicinal chemistry.
Pyrazole ring
The compound contains a pyrazole ring, which is a five-membered ring with four carbon atoms and one nitrogen atom.
Potential applications in medicinal chemistry
Due to its structural features, 1H-Pyrazolo[3,4-d]pyrimidine-3,4(2H,5H)-dione has potential applications in the field of medicinal chemistry.
Suitable scaffold for drug design
The compound's unique molecular structure makes it a suitable scaffold for drug design, meaning it can be used as a starting point for the development of new pharmaceuticals.
Exhibits biological activity
1H-Pyrazolo[3,4-d]pyrimidine-3,4(2H,5H)-dione may exhibit biological activity, meaning it could interact with biological systems and have therapeutic effects.
Interesting target for further research and development
The compound's unique molecular structure and properties make it an interesting target for further research and development in the pharmaceutical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 128850-53-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,8,5 and 0 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 128850-53:
(8*1)+(7*2)+(6*8)+(5*8)+(4*5)+(3*0)+(2*5)+(1*3)=143
143 % 10 = 3
So 128850-53-3 is a valid CAS Registry Number.
128850-53-3Relevant academic research and scientific papers
Synthesis of Certain Pyrazolopyrimidin-3-one Nucleosides
Anderson, Jack D.,Cottam, Howard B.,Larson, Steven B.,Dee Nord, L.,Revankar, Ganapathi R.,Robins, Roland K.
, p. 439 - 453 (2007/10/02)
Synthesis of the pyrazolopyrimidine-3-one congeners of guanosine, adenosine and inosine is described.Glycosylation of 3-methoxy-6-methylthio-1H-pyrazolopyrimidin-4(5H)-one (13) with 1-O-acetyl-2,3,5-tri-O-benzoyl-D-ribofuranose (16) in the p
