37634-00-7 Usage
DiaMine derivative
It contains two amino groups This indicates the presence of two NH2 groups in its structure, which contributes to its chemical reactivity and potential applications.
Pharmaceutical industry use
Building block for the synthesis of various drugs and biologically active molecules 1-Methyl-N5-phenyl-1H-1,2,4-triazole-3,5-diaMine serves as a starting material or intermediate in the creation of a wide range of pharmaceuticals due to its unique chemical structure.
Corrosion inhibitor for metals
Potential use in protecting metals from corrosion The compound may form a protective layer on metal surfaces, preventing oxidation and degradation.
Antimicrobial and antiviral properties
Examined for its ability to inhibit the growth of microorganisms and viruses This makes it a compound of interest in the development of new treatments for infections and diseases caused by various pathogens.
Interest in medicinal chemistry and drug discovery
The compound's diverse potential applications make it a valuable subject for research in the fields of medicinal chemistry and drug discovery Its unique structure and properties may lead to the development of new therapeutic agents and other useful applications.
Check Digit Verification of cas no
The CAS Registry Mumber 37634-00-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,6,3 and 4 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 37634-00:
(7*3)+(6*7)+(5*6)+(4*3)+(3*4)+(2*0)+(1*0)=117
117 % 10 = 7
So 37634-00-7 is a valid CAS Registry Number.
37634-00-7Relevant academic research and scientific papers
On Triazoles. V . Synthesis of 1- and 2-R1-3-R2,R3-Amino-5-amino-1,2,4-triazoles
Reiter, Jozsef,Pongo, Laszlo,Somorai, Tamas,Dvortsak, Peter
, p. 401 - 408 (2007/10/02)
The correct isomeric and tautomeric structure of different 1- and 2-R1-3-R2,R3-amino-5-amino-1,2,4-triazole derivatives prepared from the corresponding N-cyano-N'-R2,R3-S-methyl-isothioureas and the corresponding hydrazines was proved with the help of their ir, uv, 1H-nmr and 13C-nmr spectra as well as the uv spectra of the Schiff bases of an isomeric pair.
