196301-93-6 Usage
Uses
Used in Pharmaceutical Research and Development:
3-(4-chlorophenyl)-5-ethyl-1,2,4-oxadiazole is used as a building block for the synthesis of various biologically active molecules, contributing to the development of new drugs with potential therapeutic applications.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 3-(4-chlorophenyl)-5-ethyl-1,2,4-oxadiazole is utilized for its potential anti-inflammatory and anti-tumor properties, making it a valuable compound for the discovery and design of novel therapeutic agents.
Used in Drug Discovery:
3-(4-chlorophenyl)-5-ethyl-1,2,4-oxadiazole is employed in drug discovery processes to explore its potential as a precursor for creating new pharmaceutical compounds with improved efficacy and safety profiles.
Used in Anti-inflammatory Applications:
3-(4-chlorophenyl)-5-ethyl-1,2,4-oxadiazole is used as an anti-inflammatory agent, leveraging its potential to modulate inflammatory pathways and provide relief from inflammation-related conditions.
Used in Anti-tumor Applications:
In the context of anti-tumor applications, 3-(4-chlorophenyl)-5-ethyl-1,2,4-oxadiazole is utilized for its potential to inhibit tumor growth and progression, offering a promising avenue for cancer treatment and management.
Check Digit Verification of cas no
The CAS Registry Mumber 196301-93-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,6,3,0 and 1 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 196301-93:
(8*1)+(7*9)+(6*6)+(5*3)+(4*0)+(3*1)+(2*9)+(1*3)=146
146 % 10 = 6
So 196301-93-6 is a valid CAS Registry Number.
196301-93-6Relevant academic research and scientific papers
A novel, one-pot, three-component synthesis of 1,2,4-oxadiazoles under microwave irradiation and solvent-free conditions
Adib, Mehdi,Mahdavi, Mohammad,Mahmoodi, Niusha,Pirelahi, Hooshang,Bijanzadeh, Hamid Reza
, p. 1765 - 1767 (2008/02/04)
A novel synthesis of 3,5-disubstituted 1,2,4-oxadiazoles is described from a one-pot, three-component reaction between nitriles, hydroxylamine, and Meldrum's acids under microwave irradiation and solvent-free conditions in good to excellent yields. Georg
Ceric ammonium nitrate oxidation of aldoximes in aliphatic nitriles as solvents: A new way for synthesis of 1,2,4-oxadiazoles
Giurg,Mlochowski
, p. 1093 - 1101 (2007/10/03)
Oxidation of aromatic aldoximes with one-electron oxidant ceric ammonium nitrate CAN in acetonitrile and propionitrile, has been investigated. Aromatic nitrile oxides, formed in situ, underwent 1,3-cycloaddition with aliphatic nitriles and 5-alkyl-3-aryl-1,2,4-oxadiazoles are produced in moderate to high yields. The mechanism of the reaction based on the transformations of intermediate aldazine di-N-oxides is discussed.
