37760-49-9

Basic information

• Product Name: 3-phenyl-5-(pyridin-3-yl)-1,2,4-oxadiazole
• Synonyms: 3-phenyl-5-(pyridin-3-yl)-1,2,4-oxadiazole
• CAS NO: 37760-49-9
• Molecular Weight: 223.234
• Mol File: 37760-49-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 3-phenyl-5-(pyridin-3-yl)-1,2,4-oxadiazole(CAS DataBase Reference)
• NIST Chemistry Reference: 3-phenyl-5-(pyridin-3-yl)-1,2,4-oxadiazole(37760-49-9)
• EPA Substance Registry System: 3-phenyl-5-(pyridin-3-yl)-1,2,4-oxadiazole(37760-49-9)

Safety Data

• Hazardous Substances Data: 37760-49-9(Hazardous Substances Data)

Upstream product

• 100-54-9 pyridine-3-carbonitrile 
• 622-42-4 1-nitro-1-phenylmethane 
• 108-99-6 3-Methylpyridine 
• 1670-14-0 benzamidine monohydrochloride 
• 59-67-6 nicotinic acid 
• 3731-52-0 3-Aminomethylpyridine 
• 698-16-8 benzohydroximoyl chloride 
• 1594-58-7 nicotinamide oxime 
• 1448510-48-2 3-phenyl-5-(3-pyridyl)-1,2,4-oxadiazole-4-oxide 
• 873-67-6 benzonitrile oxide 
• 60-29-7 diethyl ether 

Relevant articles and documents

NBS-mediated practical cyclization of N-acyl amidines to 1,2,4-oxadiazoles via oxidative N?O bond formation

A reaction involving an efficient NBS-mediated oxidative N?O bond formation has been established for the synthesis of 1,2,4-oxadiazoles from readily accessible N-acyl amidines. The features of this synthetic method include simplicity of operation, mild re

A facile approach to synthesize 3,5-disubstituted-1,2,4-oxadiazoles via copper-catalyzed-cascade annulation of amidines and methylarenes

Various 3,5-disubstituted-1,2,4-oxadiazoles are smoothly formed via copper-catalyzed cascade annulation of amidines and methylarenes. This tandem oxidation-amination-cyclization transformation represents a straightforward protocol to prepare 1,2,4-oxadiazoles from easily available starting materials, with inexpensive copper catalysts and green oxidants. It has the advantages of atom- and step-economy, good functional group tolerance, as well as operational simplicity.

Synthesis of five-membered heterocycles containing a nitrogen-oxygen bond via O-acylation of aliphatic nitro compounds

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