864085-48-3

Upstream product

• 1403982-99-9 C₁₆H₁₃N₃O₄S 
• 1403982-87-5 C₁₆H₁₃N₃O₃S 
• 948854-75-9 2-phenyl-5-(2-(phenylselanyl)ethyl)-[1,3,4]oxadiazole 
• 18755-47-0 5-vinyl-1,2,3,4-tetrazole 
• 98-88-4 benzoyl chloride 

Downstream Products

• 958977-18-9 2-(3-(4-chlorophenyl)-4,5-dihydroisoxazol-5-yl)-5-phenyl-1,3,4-oxadiazole 
• 958977-46-3 2-(3-(4-fluorophenyl)-4,5-dihydroisoxazol-5-yl)-5-phenyl-1,3,4-oxadiazole 
• 958986-15-7 2-(3-(2,6-dichlorophenyl)-4,5-dihydroisoxazol-5-yl)-5-phenyl-1,3,4-oxadiazole 
• 958961-15-4 2-(3-(3-chlorophenyl)-4,5-dihydroisoxazol-5-yl)-5-phenyl-1,3,4-oxadiazole 

Relevant academic research and scientific papers

Synthesis and properties of carbon-chain polymers with pendant 1,3,4-oxadiazole rings

Carbon-chain polymers with 1,3,4-oxadiazole rings were prepared by radical polymerization and polymer-analogous transformations. The kinetic relationships of the polymerization of vinyl-1,3,4-oxadiazole monomers and some properties of the resulting polyme

A facile route for the synthesis of vinyl-substituted 1,3,4-oxadiazoles

An efficient synthesis of vinyl-substituted 1,3,4-oxadiazoles using o-nitrophenyl sulfoxide precursor via syn-elimination reaction using sodium acetate in THF is described. This method is cost effective as it uses cheap o-nitrothiophenol and can be used in the synthesis of vinyl intermediates during synthesis of bioactive compounds, which avoids the use of any toxic metals.

Solid-phase organic synthesis of vinyl-substituted 1,3,4-oxadiazoles using polymer-bound α-selenopropionic acid

Vinyl-substituted 1,3,4-oxadiazoles can be efficiently synthesized through acylation, cyclocondensation, and oxidation-elimination reaction from polystyrene-supported α-selenopropionic acid and acid hydrazides. This new solid-phase organic synthesis metho

An efficient route to vinyl substituted oxadiazoles and triazoles using phenylselanyl derivatives as precursor

Vinyl substituted oxadiazoles and triazoles were obtained from selenoxide syn-elimination of phenylselanylethyl substituted oxadiazoles and triazoles, which were prepared through hydrazinolysis, acylation, and cyclocondensation reactions of phenylselanyl-

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.