23133-34-8

Basic information

• Product Name: Phenol, 4-(5-phenyl-1,3,4-oxadiazol-2-yl)-
• CAS NO: 23133-34-8
• Molecular Formula: C14H10N2O2
• Molecular Weight: 238.246
• Mol File: 23133-34-8.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: Phenol, 4-(5-phenyl-1,3,4-oxadiazol-2-yl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Phenol, 4-(5-phenyl-1,3,4-oxadiazol-2-yl)-(23133-34-8)
• EPA Substance Registry System: Phenol, 4-(5-phenyl-1,3,4-oxadiazol-2-yl)-(23133-34-8)

Safety Data

• Hazardous Substances Data: 23133-34-8(Hazardous Substances Data)

Upstream product

• 59394-95-5 N'-[(4-hydroxyphenyl)methylidene]benzeneacylhydrazone 
• 123-08-0 4-hydroxy-benzaldehyde 
• 613-94-5 benzoic acid hydrazide 
• 99-96-7 4-hydroxy-benzoic acid 
• 5351-23-5 4-hydroxybenzoic acid hydrazide 
• 209797-66-0 Formic acid [1-ethoxy-1-phenyl-meth-(E)-ylidene]-hydrazide 
• 23048-01-3 4-acetoxy-benzoic acid N'-benzoyl-hydrazide 
• 1090-82-0 2-(4-nitrophenyl)-5-phenyl-1,3,4-oxadiazole 
• 6781-65-3 N'-benzoyl-4-nitrobenzohydrazide 
• 98-88-4 benzoyl chloride 
• 3290-99-1 4-methoxybenzoic acid hydrazide 
• 100-07-2 4-methoxy-benzoyl chloride 
• 6781-59-5 1-benzoyl-2-(4-methoxybenzoyl)hydrazine 
• 108784-49-2 benzoic acid 4-(N'-benzoyl-hydrazinocarbonyl)-phenyl ester 

Downstream Products

• 23133-32-6 1-acetoxy-4-(5-phenyl-[1,3,4]oxadiazol-2-yl)-benzene 
• 842-79-5 2-(4-methoxy-phenyl)-5-phenyl-[1,3,4]oxadiazole 
• 506424-28-8 2-(4-(4-bromobutyloxy)phenyl)-5-phenyl-[1,3,4]oxadiazole 
• 1239666-98-8 11-[4-(5-phenyl-[1,3,4]oxadiazol-2-yl)-phenoxy]-undecan-1-ol 
• 1239666-99-9 C₂₉H₃₆N₂O₄ 
• 1597428-03-9 bis[4-phenyl-2-(thiophen-2-yl)quinoline]iridium-4-(4-(5-phenyl-1,3,4-oxadiazol-2-yl)phenoxy)picolinate 
• 1252660-20-0 9-(6-(4-(5-phenyl-1,3,4-oxadiazol-2-yl)phenoxy)hexyl)-9H-carbazole 
• 335276-14-7 2-(10'-(p-(5-phenyl-1,3,4-oxadiazol-2-yl)phenoxy)decanoxy)-1,4-bis(bromomethyl)benzene 
• 929685-50-7 OXD-TPIP 
• 173865-05-9 2-methyl-acrylic acid 4-(5-phenyl-[1,3,4]oxadiazol-2-yl)phenyl ester 

Relevant articles and documents

Microwave-mediated Green synthesis of oxadiazole derivatives against inflammatory disease

A rapid and efficient microwave-mediated Green synthesis of oxadiazole derivatives (2a-e) is described based on reaction between benzohydrazide and various substituted benzoic acids. The use of microwave irradiation to carry out chemical reactions provide

2,4,6-Tris[(4-dichloroiodo)phenoxy)]-1,3,5-triazine as a new recyclable hypervalent iodine(III) reagent for chlorination and oxidation reactions

The synthesis of 2,4,6-tris[(4-dichloroiodo)phenoxy)]-1,3,5-triazine, as a new recyclable nonpolymeric analogue of (dichloroiodo)benzene, is achieved in two steps using 2,4,6-trichloro-1,3,5-triazine and 4-iodophenol. The application of 2,4,6-tris[(4-dichloroiodo)phenoxy)]-1,3,5-triazine for the chlorination reaction of various activated arenes, olefin, and 1,3-diketone is demonstrated. The reagent 2,4,6-tris[(4-dichloroiodo)phenoxy)]-1,3,5-triazine can be applied also for the oxidative synthesis of 1,3,4-oxadiazoles and 1,2,4-thiadiazoles under mild conditions in excellent yields. The recyclability of the 2,4,6-tris[(4-dichloroiodo)phenoxy)]-1,3,5-triazine was possible owing to the facile recovery and reuse of the coproduced 2,4,6-tris(4-iodophenoxy)-1,3,5- triazine from the reaction mixture due to its practical insolubility in methanol. Georg Thieme Verlag Stuttgart, New York.

The spectrophotometric study of a fluorescence-enhanced inclusion complex Threaded with β-cyclodextrin: Synthesis and characterization

A novel achiral monomer end-capped with a phenyl-[1,3,4]oxadiazolyl group and threaded through β-cyclodextrin was synthesized to investigate the host-guest interactions in the inclusion complex. 1H NMR studies revealed that one or two eyclodextrin molecules were threaded onto the synthesized achiral monomer, leading to the formation of a fibrous construction of self-assembled inclusion complexes. The formation of a self-assembled inclusion complex was identified using SEM and TEM. The highly ordered alignment of selfassembled supramolecules was confirmed using polarized optical microscopy. We demonstrate an easy process for the fabrication of nano-structured self-assembled inclusion complexes in pyridine/ethanol (1 mL/10 mL) as well as the enhancement of photo-induced fluorescence via monomers end-capped with a phenyl-[1,3,4]oxadiazolyl moiety threaded with β-cyclodextrins.