7084-55-1 Usage
Uses
Used in Pharmaceutical Industry:
2,6-diamino-5-[(4-nitrophenyl)hydrazono]pyrimidin-4(5H)-one is used as a building block for the synthesis of biologically active molecules. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
2,6-diamino-5-[(4-nitrophenyl)hydrazono]pyrimidin-4(5H)-one is used as a precursor in the synthesis of agrochemicals, such as pesticides and herbicides. Its ability to form various biologically active molecules makes it a valuable component in the development of new and effective agrochemical products.
Used in Anti-inflammatory Applications:
2,6-diamino-5-[(4-nitrophenyl)hydrazono]pyrimidin-4(5H)-one has been studied for its anti-inflammatory properties. It may be used as a therapeutic agent to treat inflammation-related conditions, although further research is needed to fully understand its potential in this area.
Used in Anti-cancer Applications:
2,6-diamino-5-[(4-nitrophenyl)hydrazono]pyrimidin-4(5H)-one has also been investigated for its anti-cancer properties. It may have potential as a chemotherapeutic agent or as a component in the development of targeted cancer therapies. However, more research is required to explore its efficacy and safety in this context.
Check Digit Verification of cas no
The CAS Registry Mumber 7084-55-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,8 and 4 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7084-55:
(6*7)+(5*0)+(4*8)+(3*4)+(2*5)+(1*5)=101
101 % 10 = 1
So 7084-55-1 is a valid CAS Registry Number.
7084-55-1Relevant 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.
