105480-49-7

Upstream product

• 63599-99-5 2,3-Dibenzoylthiophen 
• 105480-48-6 2-<3-(α-Hydroxybenzyl)-2-thienyl>-3,4,4-trimethyl-2-oxazoliniumiodid 
• 5271-67-0 2-Thiophenecarbonyl chloride 
• 527-72-0 2-thiophenylcarboxylic acid 
• 62521-42-0 4,4-dimethyl-2-(2-thienyl)oxazoline 
• 97759-72-3 N-(2-hydroxy-1,1-dimethylethyl)thiophene-2-carboxamide 
• 62521-44-2 2-<3-(α-Hydroxybenzyl)-2-thienyl>-4,4-dimethyl-2-oxazolin 
• 119639-18-8 [3-(Hydroxy-phenyl-methyl)-thiophen-2-yl]-phenyl-methanone 

Downstream Products

• 119639-21-3 exo-3a,4,8,8a-Tetrahydro-4,8-diphenyl-4,8-epoxythieno<2,3-f>-1,3-benzodioxol-2-on 
• 119639-16-6 endo-3a,4,8,8a-Tetrahydro-4,8-diphenyl-4,8-epoxythieno<2,3-f>-1,3-benzodioxol-2-on 
• 105480-50-0 2-(2-Benzoyl-3-thienyl)-4,5,6,7-tetrachlor-2-phenyl-1,3-benzodioxol 
• 105504-40-3 4,7-Dihydro-4,7-diphenyl-4,7-epoxybenzothiophen-5,6-dicarbonsaeure-dimethylester 
• 119639-20-2 C₂₉H₂₁NO₃S 
• 56138-17-1 3-ethyl-2,5-diphenylfuran 
• 119639-19-9 2-benzyl-1-phenylpentane 
• 63599-99-5 2,3-Dibenzoylthiophen 
• 119639-17-7 4,7-Diphenylbenzothiophen-6-carbonsaeure-methylester 
• 119639-23-5 4,7-Diphenylbenzothiophen-5-carbonsaeure-methylester 

Relevant academic research and scientific papers

4,6-Diphenylthienofuran

The oxazolinium iodide 9 reacts with phenylmagnesium bromide to give 4,6-diphenylthienofuran (5b).Some reactions, the X-ray structure analysis, luminescence spectra, and theoretical investigations are described. - Keywords: Thienofuran; Luminescence spectra; AM1 calculations

1,3-DIPHENYLTHIENOFURAN. A NEW HETEROCYCLIC SYSTEM

The synthesis of 1,3-diphenylthienofuran (7) is described.