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Ethyl 4-(5-phenyl-1,3,4-oxadiazol-2-yl)benzoate is a chemical compound with the molecular formula C17H13NO4. It is a derivative of benzoic acid, featuring an ethyl ester group and a 5-phenyl-1,3,4-oxadiazol-2-yl moiety. ethyl 4-(5-phenyl-1,3,4-oxadiazol-2-yl)benzoate is known for its potential applications in the synthesis of pharmaceuticals and agrochemicals due to its unique structure and reactivity. The oxadiazole ring system is a common structural motif in various biologically active molecules, making ethyl 4-(5-phenyl-1,3,4-oxadiazol-2-yl)benzoate an interesting candidate for further research and development in the field of medicinal chemistry.

1874-37-9

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1874-37-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1874-37-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,7 and 4 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1874-37:
(6*1)+(5*8)+(4*7)+(3*4)+(2*3)+(1*7)=99
99 % 10 = 9
So 1874-37-9 is a valid CAS Registry Number.

1874-37-9Downstream Products

1874-37-9Relevant academic research and scientific papers

Photocatalyzed facile synthesis of 2,5-diaryl 1,3,4-oxadiazoles with polyaniline-?g-C3N4-TiO2 composite under visible light

Wang, Liang,Wang, Yaoyao,Chen, Qun,He, Mingyang

, p. 1489 - 1492 (2018)

PANI (polyaniline)-g-C3N4-TiO2 composite was prepared and found to be efficient for the synthesis of 2,5-diaryl 1,3,4-oxadiazoles under visible light. This reaction involved decarboxylation and cyclization from α-keto acids with acylhydrazines, and a broad scope of substrates were tolerated to provide the desired products in moderate to good yields. Control experiments indicated that a radical pathway was involved in the present photocatalytic reaction and a synergistic effect may exist in the ternary composite. Moreover, this semiconductor photocatalyst could be readily recovered and showed good reusability with only slight decrease in the catalytic activity after six consecutive runs.

Palladium-Catalyzed Aminocarbonylation Reaction to Access 1,3,4-Oxadiazoles using Chloroform as the Carbon Monoxide Source

Li, Zhengyi,Wang, Liang

, p. 3469 - 3473 (2016/01/25)

A palladium-catalyzed aminocarbonylation reaction of aryl halides with chloroform and tetrazoles has been developed, where chloroform was employed as the carbon monoxide (CO) source in the presence of cesium hydroxide. The in situ generated N-acylated tetrazoles were unstable and easily decomposed to afford 2,5-disubstituted 1,3,4-oxadiazoles. A wide range of tetrazoles and aryl halides reacted smoothly under the optimized reaction conditions to give the corresponding products in moderate to good yields.

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