66902-63-4 Usage
General Description
(4-Amino-6-hydroxy-pyrimidin-2-ylsulfanyl)-acetic acid is a chemical compound with a molecular formula of C6H8N4O3S and a molecular weight of 216.22 g/mol. It is a derivative of pyrimidine and contains both an amino group and a hydroxyl group, making it potentially useful in biological and pharmaceutical applications. (4-AMINO-6-HYDROXY-PYRIMIDIN-2-YLSULFANYL)-ACETIC ACID may have the potential to act as a chelating agent, a precursor in the synthesis of pharmaceuticals, or as a building block for the development of new materials. The sulfanyl and carboxylic acid functional groups may also provide opportunities for this compound to be used in chemical reactions and organic synthesis. Overall, "(4-Amino-6-hydroxy-pyrimidin-2-ylsulfanyl)-acetic acid" has potential value in various chemical and pharmaceutical applications due to its unique structure and functional groups.
Check Digit Verification of cas no
The CAS Registry Mumber 66902-63-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,9,0 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 66902-63:
(7*6)+(6*6)+(5*9)+(4*0)+(3*2)+(2*6)+(1*3)=144
144 % 10 = 4
So 66902-63-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H7N3O3S/c7-3-1-4(10)9-6(8-3)13-2-5(11)12/h1H,2H2,(H,11,12)(H3,7,8,9,10)
66902-63-4Relevant articles and documents
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.
