40769-68-4 Usage
Uses
Used in Pharmaceutical Synthesis:
4(1H)-Pyrimidinone, 2-amino-5-hydroxy(9CI) is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to be incorporated into complex molecular structures, contributing to the development of novel therapeutic agents.
Used in Organic Chemistry:
As a building block in organic chemistry, 4(1H)-Pyrimidinone, 2-amino-5-hydroxy(9CI) is utilized for the creation of diverse chemical compounds, expanding the scope of chemical research and innovation.
Used in Antiviral Research:
4(1H)-Pyrimidinone, 2-amino-5-hydroxy(9CI) is explored for its potential antiviral properties, making it a candidate for further study and development as a therapeutic agent against viral infections.
Used in Anticancer Research:
4(1H)-Pyrimidinone, 2-amino-5-hydroxy(9CI) is also of interest in anticancer research due to its potential to target and inhibit the growth of cancer cells, offering a pathway to new cancer treatments.
Used as a Research Tool in Drug Development:
4(1H)-Pyrimidinone, 2-amino-5-hydroxy(9CI) serves as an essential research tool, aiding scientists in understanding the mechanisms of action and potential applications of new drugs and therapeutics in the medical field.
Check Digit Verification of cas no
The CAS Registry Mumber 40769-68-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,7,6 and 9 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 40769-68:
(7*4)+(6*0)+(5*7)+(4*6)+(3*9)+(2*6)+(1*8)=134
134 % 10 = 4
So 40769-68-4 is a valid CAS Registry Number.
InChI:InChI=1/C4H5N3O2/c5-4-6-1-2(8)3(9)7-4/h1,8H,(H3,5,6,7,9)
40769-68-4Relevant academic research and scientific papers
Application of the Elbs Persulfate Oxidation to the Preparation of 5-Hydroxypyrimidines
Hurst, Derek T.
, p. 1285 - 1289 (2007/10/02)
The use of potassium persulfate in cold sodium hydroxide solution has been shown to give the pyrimidin-5-yl hydrogen sulfates in cases where the pyrimidine has at least two electron-releasing groups in the 2, 4 or 6 positions.However, the reaction has been unsuccessful in a number of cases.The pyrimidin-5-yl hydrogen sulfates are hydrolysed to the corresponding 5-hydroxypyrimidines by hydrochloric acid.
