18071-11-9

Upstream product

• 1262323-90-9 C₁₇H₁₆N₄O₂ 
• 98-88-4 benzoyl chloride 
• 7256-51-1 2-(5-phenyl-1,3,4-oxadiazol-2-yl)acetonitrile 
• 938057-09-1 5-(5-phenyl-1,3,4-oxadiazol-2-ylmethyl)tetrazole 
• 16501-77-2 malonyl dihydrazide 
• 33575-83-6 2-(chloromethyl)-5-phenyl-1,3,4-oxadiazole 

Relevant academic research and scientific papers

Synthesis and evaluation of antioxidant and antibacterial activities of new substituted bis(1,3,4-oxadiazoles), 3,5-bis(substituted) pyrazoles and isoxazoles

Two series of five membered heterocyclic bis(1,3,4-oxadiazole) derivatives 2(a-h) and 3,5-bis(substituted)pyrazoles, isoxazoles 3(a,b,d-i), 4(a-c) were synthesized via oxidative cyclization of some diaroylhydrazones using chloramine-T and cyclocondensatio

Polynuclear nonfused bis(1,3,4-oxadiazole)-containing systems

Nonfused bis-1,3,4-oxadiazoles were synthesized by reaction of 5-substituted mono- and bis-tetrazoles with mono- and dicarboxylic acid chlorides. The results of kinetic studies showed that the transformation of tetrazoles into 1,3,4-oxadiazoles is accelerated by 1 to 2 orders of magnitude on addition of a catalytic amount of dimethylformamide, triethylamine, or pyridine. Pleiades Publishing, Inc., 2006.

A Convenient Synthesis of Alkyl and Aryl Substituted Bis-1,3,4-oxadiazoles

Substituted bis-1,3,4-oxadiazoles 3a-l have been synthesized from the cyclization of N,N'-diaroyl or N,N'-dialkanoyl diacyl hydrazides, in presence of phosphorus oxychloride.All new compounds have been identified by 1H-NMR, 13C-NMR and elemental analysis.