96476-07-2

Upstream product

• 96476-18-5 4-(Chlordiphenylmethyl)acetophenon 
• 96476-12-9 1-[4-({4-[(4-Acetyl-phenyl)-phenyl-methylene]-cyclohexa-2,5-dienyl}-diphenyl-methyl)-phenyl]-ethanone 
• 96476-17-4 1-(4-(hydroxydiphenylmethyl)phenyl)ethan-1-one 
• 96476-16-3 <4-(2-Methyl-1,3-dioxolan-2-yl)phenyl>diphenylmethanol 
• 99-90-1 para-bromoacetophenone 
• 4360-68-3 2-(4-bromophenyl)-2-methyl-1,3-dioxolane 

Downstream Products

• 96476-12-9 1-[4-({4-[(4-Acetyl-phenyl)-phenyl-methylene]-cyclohexa-2,5-dienyl}-diphenyl-methyl)-phenyl]-ethanone 

Relevant academic research and scientific papers

Sterically Hindered Free Radicals. 18. Stabilization of Free Radicals by Substituents As Studied by Using Triphenylmethyls

The relative stabilization of 10 4-mono- and 24 4,4'-disubstituted triphenylmethyl radicals 1 has been measured by recording the degree of dissociation of the corresponding quinonoid dimers 2 by means of ESR.The following substituents or combinations of t

Sterically Hindered Free Radicals, XIII. Wittig's Radical 4-Benzoyltriphenylmethyl and Analogous Mono-4-substituted Trityl Radicals

The mono-4-R-triphenylmethyl radicals 1, 8b-f, R = tBu, CF3, COMe, COPh, CN, Me, or their quinonoid dimers 4, 9b-f are prepared, most of them for the first time.The degree of dissociation of the latter at 25 deg C is surprisingly high (=/ 33percent, 0.01 M), donors and acceptors being effective here likewise.ESR data are given and discussed.