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2,6-diamino-pyrimidin-4,5-dione 5-[(4-methoxy-phenyl)-hydrazone] is a complex organic compound with the molecular formula C11H12N6O3. It is a derivative of pyrimidin-4,5-dione, featuring two amino groups at the 2 and 6 positions, and a hydrazone group attached to the 5 position. The hydrazone moiety is formed by the reaction of the carbonyl group at the 5 position with 4-methoxyphenylhydrazine, resulting in a C=N bond. 2,6-diamino-pyrimidin-4,5-dione 5-[(4-methoxy-phenyl)-hydrazone] is of interest in chemical research due to its potential applications in the synthesis of various pharmaceuticals and as a building block for more complex molecules. Its structure and properties make it a valuable intermediate in organic synthesis, particularly in the development of compounds with biological activity.

6979-64-2

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6979-64-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6979-64-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,7 and 9 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6979-64:
(6*6)+(5*9)+(4*7)+(3*9)+(2*6)+(1*4)=152
152 % 10 = 2
So 6979-64-2 is a valid CAS Registry Number.

6979-64-2Downstream Products

6979-64-2Relevant academic research and scientific papers

Studies on the series of azoles and azines. 66. Synthesis, spectra and structure of 5-arylazo- and 5-arylideneamino-2,4,6-triaminopyrimidines and their 6-hydroxy analogs

Belodedova,Smorygo,Mirzoyan,Melik-Orandzhanyan,Studentsov,Ivin

, p. 538 - 545 (2007/10/02)

5-Arylazo and 5-arylideneamino-2,4,6-triaminopyrimidines and their 6-hydroxy analogs were obtained by azo coupling of 2,4,6-triamino- and 2,4-diamino-6-hydroxypyrimidines with aryldiazonium salts, and also by the reaction of benzaldehydes with 2,4,5,6-tetraamino- and 2,4,5-triamino-6-hydroxypyrimidines, respectively. According to spectral data, in solvents with different polarity, these compounds exist preferentially in the triamino- or diaminohydroxy form. The main paths of the mass spectrometric fragmentation of the compounds studied have been determined.

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