38268-18-7

Upstream product

• 104-81-4 4-Methylbenzyl bromide 
• 38622-91-2 [(p-methylphenyl)sulfonylmethyl]isonitrile 
• 70769-70-9 1,3-bis(4-methylphenyl)-2-propanone 
• 134-81-6 benzil 

Downstream Products

• 80546-38-9 4,5-diphenyl-3,6-di-p-tolyl-phthalic acid-anhydride 
• 19060-00-5 3.4-Diphenyl-1.2.5-tris--cyclopentadien-(2.4)-ol-(1) 
• 79870-10-3 bis(2',5'-di-p-tolyl-4',6'-diphenyl-m-terphenyl-4-yl)ether 
• 78112-48-8 2,3-Diphenyl-1,4-di-p-tolylfluorene 
• 86997-72-0 8,9-Diphenyl-7,10-di-p-tolyl-fluoranthene 
• 78112-47-7 1,4,10,11-Tetrahydro-2,3-biphenyl-1,4-di-p-tolyl-1,4-endo-carbonylfluorene 
• 86997-87-7 6a,10a-Dihydro-8,9-diphenyl-7,10-di-(p-tolyl)-fluoranthene 
• 86997-63-9 C₄₃H₃₂O 
• 34311-81-4 1,4-Di-p-Methylphenyl-2,3-diphenylnaphthalin 
• 19057-30-8 1.3.4-Triphenyl-2.5-bis--cyclopentadien-(2.4)-yl-bromid 
• 209664-08-4 1,2,3,4,6,7-Hexaphenyl-5,8-di-p-tolyl-fluoren-9-one 
• 52954-38-8 2,3-Diphenyl-1,4-di-p-tolyl-7H-benzocycloheptene 
• 52954-40-2 6,7-Diphenyl-5,8-di-p-tolyl-7H-benzocycloheptene 

Relevant academic research and scientific papers

Efficient synthesis of substituted polyarylphthalimides via cycloaddition of cyclopentadienones with 2-bromomaleimide

Functionalized tetraarylphthalimides or diarylphthalimides fused with an acenaphthene moiety have been prepared in one step from 2-bromomaleimide and tetraarylcyclopentadienones (tetracyclones) or 7,9-diaryl-8H- cyclopentacenaphthylene-8-ones (acecyclones

Predicting the UV-vis spectra of tetraarylcyclopentadienones: Using DFT molecular orbital energies to model electronic transitions of organic materials

(Chemical Equation Presented) Tetraphenylcyclopentadienone, due to its intrinsically low HOMO-LUMO gap, has been suggested as a valuable repeat unit in conducting polymers for nanoscale electronics. The HOMO and LUMO of tetraphenylcyclopentadienone appear

Synthesis of heterosubstituted hexaarylbenzenes via asymmetric carbonylative couplings of benzyl halides

Asymmetric carbonylative couplings of benzyl halldes have been shown to give heterosubstituted 1,3-diarylacetones In moderate to high yields. These asymmetric ketones were converted via Knoevenagel condensations to tetraarylcyclopentadienones, and further