3201-50-1 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
The compound belongs to the oxadiazole class of compounds, which are characterized by a five-membered ring containing two nitrogen atoms and one oxygen atom.
Explanation
The compound contains a methoxy (-OCH3) group and a phenyl (C6H5) group, which are attached to the oxadiazole ring.
Explanation
1,2,4-Oxadiazole, 3-methoxy-5-phenylis used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds.
Explanation
The compound is being investigated for its potential use as an antiviral, antibacterial, or antifungal agent due to its possible biological activities.
Explanation
Further research is being conducted to explore the compound's properties and its potential applications in various fields, including pharmaceuticals and agrochemicals.
Class
Oxadiazole
Functional groups
Methoxy and phenyl
Applications
Intermediate in synthesis
Potential biological activities
Antiviral, antibacterial, or antifungal
Ongoing research
Properties and potential uses
Check Digit Verification of cas no
The CAS Registry Mumber 3201-50-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,0 and 1 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3201-50:
(6*3)+(5*2)+(4*0)+(3*1)+(2*5)+(1*0)=41
41 % 10 = 1
So 3201-50-1 is a valid CAS Registry Number.
3201-50-1Relevant academic research and scientific papers
Photoinduced Molecular Rearrangements. Some Investigations of the Photochemical Behavior of 3-(Acylamino)-1,2,5-Oxadiazoles (Furazans)
Buscemi, Silvestre,Vivona, Nicolo,Caronna, Tullio
, p. 4096 - 4101 (2007/10/02)
Mechanistic investigations of the photochemical behavior of some 3-(acylamino)-1,2,5-oxadiazoles (furazans) are reported.Irradiations of 3-(aroylamino)-4-methyl- and 3-(acetylamino)-4-phenyl-furazans at λ = 254 nm in methanol, and in methanol containing pyrrolidine, are considered.Photochemical processes follow different routes depending on the actual chromophore in the photoreaction.In the irradiation of 3-(aroylamino)-4-methylfurazans, two photochemical pathways involving a different multiplicity of excited states suggested: cleavage of the ring O(1)-N(5) bond via a singlet excited state (developing into nitrile oxides or carbodiimides, from which final products arise), or preliminary ring-closure involving the aroylamino group via a triplet excited state, respectively.In the irradiation of 3-(acetylamino)-4-phenylfurazan, photolytic intermediates arising from the cleavage of both the O(1)-N(2) and O(1)-N(5) bonds develop into the final products by reaction with the nucleophilic species present.
