54016-37-4 Usage
Uses
Used in Pharmaceutical Synthesis:
5-Pyrimidinol, 4,6-diamino(9CI) is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique chemical structure allows for the development of new drugs with potential therapeutic effects.
Used in Agrochemical Synthesis:
In the agrochemical industry, 5-Pyrimidinol, 4,6-diamino(9CI) serves as a building block for the creation of novel agrochemicals, such as pesticides and herbicides, that can improve crop protection and yield.
Used in Chemical Research:
5-Pyrimidinol, 4,6-diamino(9CI) is utilized in chemical research for the exploration of its potential biological activities, including anti-inflammatory and anti-tumor effects. Its versatile chemical properties make it a valuable compound for studying new mechanisms of action and potential applications in medicine.
Overall, 5-Pyrimidinol, 4,6-diamino(9CI) is a valuable chemical compound with diverse applications in the fields of chemistry, medicine, and agriculture, making it an essential component in the development of new products and therapies.
Check Digit Verification of cas no
The CAS Registry Mumber 54016-37-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,0,1 and 6 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 54016-37:
(7*5)+(6*4)+(5*0)+(4*1)+(3*6)+(2*3)+(1*7)=94
94 % 10 = 4
So 54016-37-4 is a valid CAS Registry Number.
54016-37-4Relevant 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.
