32332-99-3

Upstream product

• 100-52-7 benzaldehyde 
• 1612-76-6 2-amino-5-phenyl-1,3,4-oxadiazole 
• 1574-10-3 benzaldehyde semicarbazone 
• 613-94-5 benzoic acid hydrazide 

Downstream Products

• 176248-85-4 (5-Phenyl-[1,3,4]oxadiazol-2-yl)-(2,2,2-trichloro-1-phenyl-ethyl)-amine 
• 608127-61-3 (2-methanesulfinyl-1-phenyl-ethyl)-(5-phenyl-[1,3,4]oxadiazol-2-yl)-amine 
• 91872-99-0 2,7-Diphenyl-6-o-tolyl-6,7-dihydro-[1,3,4]oxadiazolo[3,2-a][1,3,5]triazine-5-thione 
• 91872-93-4 2,6,7-triphenyl-1,3,4-oxadiazolo<3,2-a>-s-triazine-S(6H,7H)-thion 

Relevant academic research and scientific papers

Microwave assisted synthesis and spectral analysis of schiff bases derived from 2-amino-5-aryl-1,3,4-oxadiazoles

Microwave assisted synthesis of new Schiff bases derived from 2-amino-5-substituted aryl-1,3,4-oxadiazoles with substituted aromatic aldehyde have been carried out. The chemical structures of the prepared Schiff bases have been investigated by analytical

Synthesis, spectral, thermal analyses, molecular modeling, and antimicrobial activities of Cu(II)-complexes with 1,3,4-oxadiazole Schiff-base derivatives

Seven Cu(II)-complexes with 2-amino-5-substituted aryl-1,3,4-oxadiazole Schiff bases are presented. The donors and possible geometries of the complexes were investigated by elemental and thermal (differential thermal analysis and thermogravimetric analysi

Synthesis, spectral analysis, and molecular modeling of bioactive Sn(II)-complexes with oxadiazole Schiff bases

Sn(II)-complexes of seven 2-amino-5-substituted-aryl-1,3,4-oxadiazole Schiff bases have been synthesized and characterized by various physico-chemical studies. Their structures have been confirmed by elemental analyses, infrared, 1H NMR, UV-Vis, and mass

A new route for the convenient synthesis of imidazo[2,1-b]-1,3,4-oxadiazoles and their fungitoxicity

5-Aryl-1-arylideneamino-1,3,4-oxadiazoles (4a-f) react with trichloroacetic acid with the evolution of carbon dioxide to furnish 5-aryl-2-[(1-aryl-2,2,2-trichloroethyl)amino]-1,3,4-oxadiazoles (6a-f), which undergo ring closure with primary arylamines to

Synthesis of Some 1-(5'-Substituted phenyl-1',3',4'-oxadiazol-2'-yl)-3-chloro-4-substituted-2-azetidinones as Antibacterial and Antifungal Agents

Several 1-(5'-substituted phenyl-1',3',4'-oxadiazol-2'-yl)-3-chloro-4-substituted-2-azetidinones were synthesized by annulation of an acid on anils using POCl3 and Et3N and of an acid chloride on anils using Et3N.Their antibacterial and antifungal activit