3206-36-8 Usage
Family
Oxadiazole
It belongs to the oxadiazole family, which is known for its diverse range of pharmacological activities.
Ethoxy group
-OC2H5
The presence of an ethoxy group in the compound contributes to its chemical and biological properties.
4-Nitrophenyl group
-C6H4NO2
The 4-nitrophenyl group is another key structural feature of 1,3,4-Oxadiazole, 2-ethoxy-5-(4-nitrophenyl)-, influencing its properties and potential applications.
Potential applications
Pharmaceuticals, agrochemicals, and new materials
1,3,4-Oxadiazole, 2-ethoxy-5-(4-nitrophenyl)- has been studied for its potential use in various fields, including the development of pharmaceuticals, agrochemicals, and new materials.
Unique structure
Interest for further research and practical applications
The compound's unique structure and properties make it a subject of interest for ongoing research and potential practical applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 3206-36-8 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 6 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3206-36:
(6*3)+(5*2)+(4*0)+(3*6)+(2*3)+(1*6)=58
58 % 10 = 8
So 3206-36-8 is a valid CAS Registry Number.
3206-36-8Relevant academic research and scientific papers
Application of N-Acylbenzotriazoles in the Synthesis of 5-Substituted 2-Ethoxy-1,3,4-oxadiazoles as Building Blocks toward 3,5-Disubstituted 1,3,4-Oxadiazol-2(3H)-ones
Wet-Osot, Sirawit,Phakhodee, Wong,Pattarawarapan, Mookda
, p. 9923 - 9929 (2017/09/23)
5-Substituted-2-ethoxy-1,3,4-oxadiazoles were conveniently prepared through a one-pot sequential N-acylation/dehydrative cyclization between ethyl carbazate and N-acylbenzotriazoles in the presence of Ph3P-I2 as a dehydrating agent. Subsequent treatment with a stoichiometric amount of alkyl halides (X = Cl, Br, I) enables a rapid access to a variety of 3,5-disubstituted 1,3,4-oxadiazol-2(3H)-ones in good to excellent yields.
