36162-16-0 Usage
Uses
Used in Pharmaceutical Industry:
Ethyl [(6-amino-4-oxo-1,4-dihydropyrimidin-2-yl)sulfanyl]acetate is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure and properties make it a promising candidate for the development of drugs for the treatment of various diseases.
Used in Drug Development:
Ethyl [(6-amino-4-oxo-1,4-dihydropyrimidin-2-yl)sulfanyl]acetate is used as a key component in the development of new drugs. Its potential biological activity and unique structure make it a valuable compound for research and development efforts in the pharmaceutical industry.
Used in Research and Development:
Ethyl [(6-amino-4-oxo-1,4-dihydropyrimidin-2-yl)sulfanyl]acetate is used as a research compound to explore its potential applications and properties. Its unique structure and potential biological activity make it an interesting subject for future studies and development efforts in the pharmaceutical field.
Check Digit Verification of cas no
The CAS Registry Mumber 36162-16-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,1,6 and 2 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 36162-16:
(7*3)+(6*6)+(5*1)+(4*6)+(3*2)+(2*1)+(1*6)=100
100 % 10 = 0
So 36162-16-0 is a valid CAS Registry Number.
36162-16-0Relevant academic research and scientific papers
Chemical synthesis of some novel 6-aminouracil-2-thiones and their glycoside analogues
Gaafar,Aly,Abu-Zied, Khadiga M.,Abdel-Rahman, Asmaa E.,Helmy
, p. 779 - 797 (2017/04/17)
6-AMINOURACIL-2-THIONE (1) and its 5-bromo derivative 2 underwent alkylation yielding their respective S-alkyl products 4a-j. The reaction of compound 1 and aldehydes in the presence of chloroacetic acid afforded the respective thiazolopyrimidinyl acetamides 7a-d. The C-glycosides 8a, b and 9c-e were successfully prepared through condensing compound 1 and the appropriate sugar in the presence of chloroacetic acid. The behavior of certain S-alkyl derivative 4 towards amines and hydrazines was also studied. Structure elucidations for the new products were supported by compatible chemical and spectral measurements.
