24447-14-1

Usage

Molecular structure

2,5-di(thiophen-2-yl)-1,3,4-oxadiazole consists of a five-membered 1,3,4-oxadiazole ring with two thiophene groups attached to the second position of the thiophene rings.

Building block

It is a common building block in the synthesis of organic electronic materials, such as organic light-emitting diodes (OLEDs) and organic photovoltaic cells (OPVs).

Electron affinity

The compound possesses good electron affinity.

Electron-transport material

It is often used as an electron-transport material in organic electronic devices.

Structural and electronic properties

The unique structural and electronic properties of 2,5-di(thiophen-2-yl)-1,3,4-oxadiazole make it a valuable component in the development of advanced materials for electronic applications.

Upstream product

• 527-72-0 2-thiophenylcarboxylic acid 
• 2361-27-5 2-thienylhydrazide 
• 24499-57-8 N'-(thiophene-2-carbonyl)thiophene-2-carbohydrazide 
• 5271-67-0 2-Thiophenecarbonyl chloride 
• 132500-90-4 C₁₄H₁₄N₄O₄S₂ 

Relevant academic research and scientific papers

Improved synthesis of oxadiazoles under microwave irradiation

Amidoximes reacted with isopropenyl acetate in presence of KSF under microwave irradiation and gave 1,2,4-oxadiazoles. 1,2,4-Oxadiazoles can also be obtained by microwave irradiation from O-acetylamidoximes absorbed on Alumina. 1,3,4-Oxadiazoles were obta

Synthesis method of 2,5-disubstituted-1,3,4-oxadiazole

The invention discloses a synthesis method of a drug intermediate, namely, 2,5-disubstituted-1,3,4-oxadiazole. 2,5-disubstituted-1,3,4-oxadiazole is synthesized with a one-pot method under the photocatalytic action with simple hydrazide compounds as raw materials. 2,5-disubstituted-1,3,4-oxadiazole can be produced through a reaction at the room temperature with a common halogen lamp as a light source, eosinY as a catalyst, potassium carbonate as an additive and ethanol as a solvent. The method has the characteristics that the raw material source is simple, the reaction condition is mild and the like.

A new synthesis of symmetrical 2,5-disubstituted 1,3,4- oxadiazoles

Several new 2,5-disubstituted 1,3,4-oxadiazoles have been synthesized in good yields by reaction of aromatic acids with hydrazine dihydrochloride in a mixture of orthophosphoric acid, phosphorus pentoxide and, in general, with addition of phosphorus oxychloride to the reaction mixture. The structures of new oxadiazoles derivatives were confirmed by analytical and spectral data.

SYNTHESE D'OXADIAZOLES ET D'OXAZOLES THIOPHENIQUES

Some potentially active drugs: oxadiazoles (4, 8, 17), oxazoles (10, 12a, 12b, 13) heterocycles substituted by a thiophenic moiety have been prepared by a multistep procedure. Key words: Thiophene; oxadiazole; oxazole; potentially active drugs.

Unusual Rearrangement in the Dehydration of Aroylated Butanodihydrazides

Dehydration of N,N'-diaroylbutanodihydrazides 3a-f with phosphoryl chloride gave, unexpectedly, 2,5-diaryl-1,3,4-oxadiazoles 4a-f.However, dehydration of N,N'-dialkanoylbutanodihydrazides 1a-c afforded 5,5'-dialkyl-2,2'-(ethandiyl)-bis(1,3,4-oxadiazoles) 2a-c. Key Words: 1,3,4-Oxadiazole / Butanodihydrazides

N,N-Dimethylchlorosulfitemethaniminium chloride as a dehydrating agent - An efficient one-pot synthesis of 1,3,4-oxadiazoles and 4H-3,1-benzoxazin-4-ones

Aroylhydrazines (3) on treatment with carboxylic acids (1) in the presence of N,N-dimethylchlorosulfitemethaniminium chloride (2) yields directly 1,3,4-oxadiazoles (4).Reaction between anthranilic acid (6) and carboxylic acids (5) in the presence of 2 affords 4H-3,1-benzoxazin-4-ones (7).