405313-64-6

Upstream product

• 98-51-1 4-tert-butyltoluene 

Downstream Products

• 1227674-35-2 4-tert-butyl-2,6-diiodobenzyl alcohol 
• 1227674-33-0 (2,6-dibromo-4-tert-butylphenyl)(2,6-diiodo-4-tert-butylphenyl)methyl radical 
• 1227674-47-6 (2,6-dibromo-4-tert-butylphenyl)(2-iodo-4-tert-butylphenyl)methyl methyl eter 
• 1227674-46-5 C₂₂H₂₆Br₂I₂O 
• 1227674-45-4 (2,6-dibromo-4-tert-butylphenyl)(2-iodo-4-tert-butylphenyl)methane 
• 1227674-44-3 C₂₁H₂₄Br₂I₂ 
• 1227674-43-2 C₂₁H₂₂Br₂I₂O 
• 1227674-32-9 (2,6-dibromo-4-tert-butylphenyl)(2,6-diiodo-4-tert-butylphenyl)diazomethane 
• 1227674-40-9 ethyl N-nitroso-N-[(2,6-dibromo-4-tert-butylphenyl)(2,6-diiodo-4-tert-butylphenyl)methyl]carbamate 
• 1227674-39-6 ethyl N-[(2,6-dibromo-4-tert-butylphenyl)(2,6-diiodo-4-tert-butylphenyl)methyl]carbamate 
• 1227674-38-5 (2,6-dibromo-4-tert-butylphenyl)(2,6-diiodo-4-tertbutylphenyl)chloromethane 
• 1227674-37-4 (2,6-dibromo-4-tert-butylphenyl)(2,6-diiodo-4-tert-butylphenyl)methanol 
• 1227674-34-1 4-tert-butyl-2,6-diiodobenzyl acetate 
• 464895-80-5 1-(4,4-diphenylbut-3-en-1-ynyl)-5-(tert-butyl)-3-iodo-2-methylbenzene 

Relevant academic research and scientific papers

Increased activity of in situ catalysts for alkyne metathesis

(figure presented) Reaction of an enyne (1,1-diphenyl-pent-1-ene-3-yne) with a preheated mixture of Mo(CO)6/4-chlorophenol/3-hexyne at 130 °C furnished 1,1,6,6-tetraphenylhex-1,5-diene-3-yne in an 80% yield. If the starting material was heated

A d3h-symmetric macrocycle alternatingly composed of pyridine and benzyl alcohol units linked with acetylene bonds

A macrocyclic compound alternatingly composed of three pyridine and three benzyl alcohol units linked with acetylene bonds was developed as a new type of D3h-symmetric hexagonal shape-persistent macrocycles with a host function. The macrocycle was prepare

Progressive direct iodination of sterically hindered alkyl substituted benzenes

Benzene derivatives bearing at least one bulky alkyl group (i-Pr or t-Bu) were selectively and effectively iodinated using elemental iodine activated, by 1-(chloromethyl)-4-fluoro-1,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate) (Selectfluor, F-TED