54559-45-4 Usage
Description
(4,5-Diphenyl-4H-[1,2,4]triazol-3-ylsulfanyl)-acetic acid is a chemical compound that belongs to the class of triazoles, known for their diverse biological activities. (4,5-DIPHENYL-4 H-[1,2,4]TRIAZOL-3-YLSULFANYL)-ACETIC ACID features a sulfur-containing group, which may provide unique properties such as antioxidant, antimicrobial, or metal chelating abilities. The presence of diphenyl groups suggests potential for interactions with biological targets, making it a promising candidate for drug development. Additionally, the acetic acid moiety may contribute to water solubility, which is important for pharmaceutical formulations. Overall, this compound represents an interesting subject for further research and potential applications in medicinal and industrial chemistry.
Uses
Used in Pharmaceutical Industry:
(4,5-Diphenyl-4H-[1,2,4]triazol-3-ylsulfanyl)-acetic acid is used as a potential pharmaceutical candidate for various applications due to its diverse biological activities and unique properties.
Used in Industrial Chemistry:
(4,5-Diphenyl-4H-[1,2,4]triazol-3-ylsulfanyl)-acetic acid is used as a compound with potential applications in industrial chemistry, particularly for its unique properties and interactions with biological targets.
Used in Antioxidant Applications:
(4,5-Diphenyl-4H-[1,2,4]triazol-3-ylsulfanyl)-acetic acid is used as an antioxidant agent, leveraging its sulfur-containing group to provide protection against oxidative stress and related cellular damage.
Used in Antimicrobial Applications:
(4,5-Diphenyl-4H-[1,2,4]triazol-3-ylsulfanyl)-acetic acid is used as an antimicrobial agent, potentially offering a new approach to combat resistant bacteria and other microorganisms.
Used in Metal Chelating Applications:
(4,5-Diphenyl-4H-[1,2,4]triazol-3-ylsulfanyl)-acetic acid is used as a metal chelating agent, which can be beneficial in various industrial processes and environmental applications.
Used in Drug Development:
(4,5-Diphenyl-4H-[1,2,4]triazol-3-ylsulfanyl)-acetic acid is used as a compound for drug development, with its diphenyl groups and acetic acid moiety potentially allowing for interactions with biological targets and improved water solubility for pharmaceutical formulations.
Check Digit Verification of cas no
The CAS Registry Mumber 54559-45-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,5,5 and 9 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 54559-45:
(7*5)+(6*4)+(5*5)+(4*5)+(3*9)+(2*4)+(1*5)=144
144 % 10 = 4
So 54559-45-4 is a valid CAS Registry Number.
InChI:InChI=1/C16H13N3O2S/c20-14(21)11-22-16-18-17-15(12-7-3-1-4-8-12)19(16)13-9-5-2-6-10-13/h1-10H,11H2,(H,20,21)
54559-45-4Relevant articles and documents
Synthesis and antimicrobial evaluation of some novel 1,2,4-triazole and 1,3,4-thiadiazole derivatives
Popiolek, Lukasz,Kosikowska, Urszula,Mazur, Liliana,Dobosz, Maria,Malm, Anna
, p. 3134 - 3147 (2013/07/11)
This study presents the synthesis and spectral analysis of new derivatives of 1,2,4-triazole-3-thione and 1,3,4-thiadiazole. New compounds were prepared by cyclization reaction of acyl thiosemicarbazide derivatives in the presence of alkaline and acidic media. All synthesized compounds were screened for their in vitro antibacterial activity by using the agar dilution technique. Six of the compounds had potential activity against Gram-positive bacteria (minimal inhibitory concentration [MIC] = 15.63-500 μg/mL). Some compounds showed good activity especially against Bacillus subtilis ATCC 6633 (MIC = 15.63-250 μg/mL), Staphylococcus aureus ATCC 25923 (MIC = 31.25-250 μg/mL), and Micrococcus luteus ATCC 10240 (MIC = 125-250 μg/mL).
