6683-74-5

Upstream product

• 1012-72-2 1,4-di-tert-butylbenzene 
• 21860-03-7 2,5-di-tert-butylaniline 
• 71-43-2 benzene 
• 253185-03-4 tert-butylbenzene 
• 7726-95-6 bromine 

Downstream Products

• 31603-97-1 2-tert.-Butyloxy-1,4-di-tert.-butyl-benzol 
• 117828-86-1 2,5-Di-tert-butyldithiobenzoesaeure-methylester 
• 38393-97-4 5-(tert-butyl)-1,1-dimethyl-2,3-dihydro-1H-indene 
• 22875-50-9 2,5,2',5'-Tetra-tert.-butyl-benzhydrol 
• 22875-49-6 2,5,2',5'-Tetra-tert.-butyl-benzophenon 
• 22875-48-5 2,5-Di-tert.-butyl-benzamid 
• 19862-71-6 Bis-<2,5-di-tert.butyl-phenyl>-disulfid 
• 7515-32-4 Bis-<2,5-di-tert.-butyl-phenyl>-methan 
• 253336-43-5 2,5-di-tert-butylphenylsilanetriol 
• 97135-80-3 C₁₈H₂₁⁽²⁾H₉ 
• 1012-72-2 1,4-di-tert-butylbenzene 
• 5875-45-6 2,5-di-tert-butylphenol 
• 1459-11-6 1,2,4-tri-tert-butylbenzene 
• 97135-79-0 2,2',5,5'-tetra-tert-butylbiphenyl 

Relevant academic research and scientific papers

2,5-Di-tert-butylphenylsilanetriol: Synthesis and reactivity

Stable 2,5-di-tert-butylphenylsilanetriol was prepared by a stepwise synthesis. This compound reacted with triethylenediamine and lanthanum silylamide to form a 1 : 1 molecular complex and highly thermally stable lanthanosilsesquioxane, respectively.

Formation of Persistent Benzyl Radicals by Protonation of the Radical Anions of Sterically Hindered Dithiobenzoic Esters

ESR signals due to a second species are observed besides the spectra of the corresponding radical anions when the methyl ortho-(tert-butyl)dithiobenzoates 1, 4, and 6 are electroreduced in situ in dimethylformamide.It is shown by investigation of model co