109519-47-3 Usage
Uses
Used in Pharmaceutical Research and Development:
Methyl 2,5-dihydro-5-oxo-1-phenyl-1H-1,2,4-triazole-3-carboxylate is utilized as a key intermediate in the synthesis of potential drug molecules, particularly for the development of new antimicrobial, antifungal, and antitumor agents. Its unique chemical structure and biological activities make it a valuable compound in the discovery and design of novel therapeutics.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, Methyl 2,5-dihydro-5-oxo-1-phenyl-1H-1,2,4-triazole-3-carboxylate serves as a building block for the creation of new chemical entities with potential therapeutic applications. Its versatile chemical properties allow for various modifications and functionalizations, enabling the development of innovative drug candidates with improved efficacy and selectivity.
Used in Antimicrobial Applications:
Methyl 2,5-dihydro-5-oxo-1-phenyl-1H-1,2,4-triazole-3-carboxylate is employed as an antimicrobial agent, targeting a wide range of bacteria and inhibiting their growth and proliferation. Its ability to disrupt essential cellular processes in bacteria makes it a promising candidate for the development of new antibiotics to combat drug-resistant infections.
Used in Antifungal Applications:
As an antifungal agent, Methyl 2,5-dihydro-5-oxo-1-phenyl-1H-1,2,4-triazole-3-carboxylate exhibits potent activity against various fungal species, interfering with their cellular functions and preventing their growth. This property makes it a valuable component in the development of new antifungal drugs to treat fungal infections and combat drug-resistant strains.
Used in Antitumor Applications:
Methyl 2,5-dihydro-5-oxo-1-phenyl-1H-1,2,4-triazole-3-carboxylate has been studied for its potential antitumor properties, showing promise as a chemotherapeutic agent. Its ability to target and inhibit the growth of cancer cells, as well as its potential to enhance the effectiveness of existing cancer treatments, makes it a valuable compound in the search for novel anticancer drugs.
Check Digit Verification of cas no
The CAS Registry Mumber 109519-47-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,5,1 and 9 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 109519-47:
(8*1)+(7*0)+(6*9)+(5*5)+(4*1)+(3*9)+(2*4)+(1*7)=133
133 % 10 = 3
So 109519-47-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H9N3O3/c1-16-9(14)8-11-10(15)13(12-8)7-5-3-2-4-6-7/h2-6H,1H3,(H,11,12,15)
109519-47-3Relevant academic research and scientific papers
Reaction of C-(Triphenylphosphinimido)hydrazones with Isocyanates as a Route to 5-Arylamino- and 5-Alkylamino-1H-1,2,4-triazoles
Bruche, Luca,Garanti, Luisa,Zecchi, Gaetano
, p. 2177 - 2180 (2007/10/02)
Treatment of C-(triphenylphosphinimido)hydrazone (1) with aryl and alkyl isocyanates results in 5-arylamino- and 5-alkylamino-1H-1,2,4-triazoles (5), often accompanied by a minor quantity of the triazol-5-one (7).The related ortho-acyl-substituted substrates (8) react with phenyl isocyanate to give triazoloquinazolines (12) or (13) through the intermediacy of aminotriazoles (11).
