113056-45-4 Usage
Uses
Used in Pharmaceutical Industry:
5-(4-CHLORO-PHENOXYMETHYL)-4H-[1,2,4]TRIAZOLE-3-THIOL is used as a pharmaceutical agent for its antimicrobial, antifungal, and antiparasitic properties. It is employed in the development of new drugs to combat various infections and diseases caused by microorganisms and parasites.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 5-(4-CHLORO-PHENOXYMETHYL)-4H-[1,2,4]TRIAZOLE-3-THIOL serves as a key compound for research and development. Its unique structure and potential biological activities make it a valuable candidate for designing and synthesizing new therapeutic agents with improved efficacy and safety profiles.
Used in Drug Development:
5-(4-CHLORO-PHENOXYMETHYL)-4H-[1,2,4]TRIAZOLE-3-THIOL is utilized in drug development as a lead compound for the discovery of novel therapeutic agents. Its potential applications in treating various diseases and conditions make it a promising candidate for further investigation and optimization to enhance its pharmacological properties and reduce potential side effects.
Used in Antimicrobial Applications:
5-(4-CHLORO-PHENOXYMETHYL)-4H-[1,2,4]TRIAZOLE-3-THIOL is used as an antimicrobial agent to combat bacterial infections. Its ability to inhibit the growth and proliferation of bacteria makes it a valuable tool in the development of new antibiotics to address the growing issue of antibiotic resistance.
Used in Antifungal Applications:
In the realm of antifungal treatments, 5-(4-CHLORO-PHENOXYMETHYL)-4H-[1,2,4]TRIAZOLE-3-THIOL is employed as an antifungal agent to treat fungal infections. Its potential to inhibit fungal growth and prevent the spread of infections contributes to the development of new antifungal drugs to address various fungal diseases.
Used in Antiparasitic Applications:
5-(4-CHLORO-PHENOXYMETHYL)-4H-[1,2,4]TRIAZOLE-3-THIOL is utilized as an antiparasitic agent to target and eliminate parasites causing various diseases. Its potential to disrupt the life cycle and survival of parasites makes it a promising candidate for the development of new antiparasitic drugs to treat parasitic infections.
Check Digit Verification of cas no
The CAS Registry Mumber 113056-45-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,0,5 and 6 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 113056-45:
(8*1)+(7*1)+(6*3)+(5*0)+(4*5)+(3*6)+(2*4)+(1*5)=84
84 % 10 = 4
So 113056-45-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H8ClN3OS/c10-6-1-3-7(4-2-6)14-5-8-11-9(15)13-12-8/h1-4H,5H2,(H2,11,12,13,15)
113056-45-4Relevant academic research and scientific papers
Synthesis and characterization of biologically important quinoline incorporated triazole derivatives
D'Souza, Vineetha Telma,Nayak, Janardhana,D'Mello, Desmond Edward,Dayananda
, (2020/11/04)
Triazoles are well recognized in literature for their significant biologically active heterocyclic compounds. Also the quinoline nucleus found in several natural products shows a varied biological activity. Keeping in the view of these observations, a novel series of 6/7/8-substtuted-2-[(5-((4-chlorophenoxy)methyl)-4H-1,2,4-triazol-3-yl)thio]quinoline-3-carbaldehydes and 6/7/8-substituted-2-[(5-(pyridin-4-yl)-4H-1,2,4-triazol-3-yl)thio]quinoline-carbaldehydes were synthesized by the condensation of 5-(4-chloro phenoxy methyl)-2,4-dihydro-1,2,4-triazole-3-thiones and 5-(pyridin-3-yl)-4H-1,2,4-triazole-3-thiols with 6/7/8-substituted-2-chloro quinoline-3-carbaldehydes. The new series were established by Mass, NMR and IR spectroscopy and were also screened for their antimicrobial activities. A few of the novel compounds exhibited tremendous bioactivities compared to that of normal drug.
