107952-08-9 Usage
Uses
Used in Medicinal Chemistry:
2,4-Dihydro-4-(4-ethoxyphenyl)-5-((2-methoxyphenoxy)methyl)-3H-1,2,4-triazole-3-thione is used as a lead molecule for the development of new therapeutic agents due to its potential pharmacological activities. Its structural features suggest it may possess antifungal, antibacterial, or antiproliferative properties, making it a promising candidate for further research and development in the pharmaceutical industry.
Used in Synthetic and Organic Chemistry:
2,4-Dihydro-4-(4-ethoxyphenyl)-5-((2-methoxyphenoxy)methyl)-3H-1,2,4-t riazole-3-thione is also used as a subject of interest for synthetic and organic chemists. Its structural complexity and the presence of diverse functional groups make it an intriguing target for exploring novel chemical reactions and developing innovative methods for its synthesis. The study of 2,4-Dihydro-4-(4-ethoxyphenyl)-5-((2-methoxyphenoxy)methyl)-3H-1,2,4-t riazole-3-thione could contribute to advancements in chemical synthesis techniques and the discovery of new synthetic pathways.
Further research and investigation are essential to fully understand the potential uses and properties of 2,4-Dihydro-4-(4-ethoxyphenyl)-5-((2-methoxyphenoxy)methyl)-3H-1,2,4-triazole-3-thione, ensuring its potential is harnessed effectively across various scientific disciplines.
Check Digit Verification of cas no
The CAS Registry Mumber 107952-08-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,9,5 and 2 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 107952-08:
(8*1)+(7*0)+(6*7)+(5*9)+(4*5)+(3*2)+(2*0)+(1*8)=129
129 % 10 = 9
So 107952-08-9 is a valid CAS Registry Number.
InChI:InChI=1/C18H19N3O3S/c1-3-23-14-10-8-13(9-11-14)21-17(19-20-18(21)25)12-24-16-7-5-4-6-15(16)22-2/h4-11H,3,12H2,1-2H3,(H,20,25)
107952-08-9Relevant academic research and scientific papers
Synthesis of Some New Substituted Mercaptotriazoles and Thiazolidones and Their Monoamine Oxidase Inhibitory and Anticonvulsant Properties
Husain, M. I.,Amir, Mohd,Singh, Eira
, p. 251 - 254 (2007/10/02)
A number of 4-aryl-5-aryloxymethyl-3-mercapto-1,2,4(H)-triazoles (IV) and 2-arylimino-3-aryloxyacetamido-4-thiazolidones (V) have been synthesized.Some of these compounds inhibit rat brain monoamine oxidase (MAO) in vitro at a final concentration of 1E-3 mol/litre, but are found to be inactive against pentylenetetrazole induced seizures in mice at a dose of 80 mg/kg.
Synthesis of some New Substituted Thiosemicarbazides and Triazoles as Possible Anticonvulsants
Husain, M. I.,Amir, Mohd.
, p. 317 - 319 (2007/10/02)
Forteen 1-o/p-anisoxyacetyl-4-arylthiosemicarbazides and their corresponding 5-(o/p-anisoxymethyl)-4-aryl-3-mercapto-1,2,4(H)-triazoles were synthesized.Eight of these compounds, when screened against maximal electroshock and pentylenetetrazole-induced seizures in mice at a dose of 80 mg/kg were, however, found to be inactive.
