62681-97-4 Usage
Uses
Used in Pharmaceutical and Agrochemical Industries:
2-(3-Fluorophenyl)-5-phenyl-1,3,4-oxadiazole is used as a chemical building block for the synthesis of various pharmaceutical and agrochemical compounds due to its ability to modulate biological targets and contribute to the development of new drugs and pesticides.
Used in Medicinal Chemistry and Drug Discovery:
In the field of medicinal chemistry, 2-(3-Fluorophenyl)-5-phenyl-1,3,4-oxadiazole is utilized as a key component in the design and synthesis of potential drug candidates, leveraging its interaction with biological targets to address various medical conditions.
Used in Antimicrobial Applications:
2-(3-Fluorophenyl)-5-phenyl-1,3,4-oxadiazole is employed as an antimicrobial agent, demonstrating effectiveness against a range of microorganisms, thereby contributing to the development of new antimicrobial therapies.
Used in Anti-Inflammatory Applications:
2-(3-Fluorophenyl)-5-phenyl-1,3,4-oxadiazole is used as an anti-inflammatory agent, potentially mitigating inflammation and related conditions, offering a new avenue for the treatment of inflammatory diseases.
Used in Anticancer Applications:
2-(3-Fluorophenyl)-5-phenyl-1,3,4-oxadiazole is used as an anticancer agent, showing promise in targeting and inhibiting the growth of cancer cells, thus contributing to the advancement of cancer therapeutics.
Used in Analytical Chemistry as a Fluorescent Probe:
In the field of analytical chemistry, 2-(3-Fluorophenyl)-5-phenyl-1,3,4-oxadiazole is used as a fluorescent probe for detecting metal ions and analyzing biological samples, providing a sensitive and selective tool for various analytical applications.
Check Digit Verification of cas no
The CAS Registry Mumber 62681-97-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,6,8 and 1 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 62681-97:
(7*6)+(6*2)+(5*6)+(4*8)+(3*1)+(2*9)+(1*7)=144
144 % 10 = 4
So 62681-97-4 is a valid CAS Registry Number.
62681-97-4Relevant academic research and scientific papers
Cu(II) catalyzed imine C-H functionalization leading to synthesis of 2,5-substituted 1,3,4-oxadiazoles
Guin, Srimanta,Ghosh, Tuhin,Rout, Saroj Kumar,Banerjee, Arghya,Patel, Bhisma K.
, p. 5976 - 5979 (2012/01/02)
A direct access to symmetrical and unsymmetrical 2,5-disubstituted [1,3,4]-oxadiazoles has been accomplished through an imine C-H functionalization of N-arylidenearoylhydrazide using a catalytic quantity of Cu(OTf)2. This is the first example of amidic oxygen functioning as a nucleophile in a Cu-catalyzed oxidative coupling of an imine C-H bond. These reactions can be performed in air atmosphere and moisture making it exceptionally practical for application in organic synthesis.
1,3,4-Oxadiazole formation as traceless release in solid phase organic synthesis
Cesarini, Sara,Colombo, Nicoletta,Pulici, Maurizio,Felder, Eduard R.,Brill, Wolfgang K.-D.
, p. 10223 - 10236 (2007/10/03)
Oxadiazoles were generated upon a dehydrative cyclization reaction with 2-acyl hydrazides bound to the polymeric support via one of their N atoms using TFAA as a dehydration agent.
