864085-48-3

Basic information

• Product Name: 2-PHENYL-5-VINYL-1,3,4-OXADIAZOLE
• Synonyms: 2-PHENYL-5-VINYL-1,3,4-OXADIAZOLE
• CAS NO: 864085-48-3
• Molecular Formula: C₁₀H₈N₂O
• Molecular Weight: 172.18
• Mol File: 864085-48-3.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 2-PHENYL-5-VINYL-1,3,4-OXADIAZOLE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-PHENYL-5-VINYL-1,3,4-OXADIAZOLE(864085-48-3)
• EPA Substance Registry System: 2-PHENYL-5-VINYL-1,3,4-OXADIAZOLE(864085-48-3)

Safety Data

• Hazardous Substances Data: 864085-48-3(Hazardous Substances Data)

Upstream product

• 1403982-87-5 C₁₆H₁₃N₃O₃S 
• 1403982-99-9 C₁₆H₁₃N₃O₄S 
• 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 articles and documents

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

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

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.