156360-14-4

Upstream product

• 110-00-9 furan 
• 113101-90-9 2,6-di-tert-butyl-4-iodo-1-<(trimethylsilyl)oxy>benzene 
• 81745-86-0 2-furylzinc chloride 

Downstream Products

• 156360-17-7 2,5-Bis-(3,5-di-tert-butyl-4-trimethylsilanyloxy-phenyl)-furan 
• 84374-65-2 2,6-di(t-butyl)-4-(2'-furyl)phenol 
• 172424-62-3 5,5'-bis(3,5-di-tert-butyl-4-hydroxyphenyl)-2,2'-bifuran 
• 172424-61-2 5,5'-bis(3,5-di-tert-butyl-4-(silyloxy)phenyl)-2,2'-bifuran 
• 156360-15-5 C₃₂H₄₄O₃ 
• 156360-19-9 C₃₂H₄₂O₃ 
• 2455-14-3 3,5,3',5'-tetra-tert-butyl-4,4'-diphenoquinone 
• 172424-60-1 2-bromo-5-(3,5-di-tert-butyl-4-(trimethylsiloxy)phenyl)furan 

Relevant academic research and scientific papers

A convenient synthesis of heteroquaterphenoquinones including novel nitrogen- and selenium-containing quinones with characteristic properties

A series of heteroquaterphenoquinones including novel biselenieno- and bi-N-methylpyrrolo-quinonoid incorporated quinones have been synthesized by a novel one-pot oxidative homocoupling reaction of heterocycle-substituted phenols.Characteristic properties adequate for using as functional materials have been clarified.

Synthesis of novel heteroquaterphenoquinones and their electrochemical, structural, and spectroscopic characterization

Novel heteroquaterphenoquinones, 5,5′-bis(3,5-di-tert-butyl-4-oxo-2,5-cyclohexadien-1-ylidene)-5,5′- dihydro-2,2′-bithienyl (3) and its 2,2′-biselenienyl (4), 2,2′-bifuryl (5), and 2,2′-bi-N-methylpyrrolyl (6) analogues, were synthesized by a stepwise cro

Novel Amphoteric 2,5-Furoquinonoid-Containing p-Terphenoquinone Analogues Giving Both a Stable Radical Anion and a Stable Radical Cation

Novel p-terphenoquinone analogues incorporating a central dihydrofurandiylidene skeleton have been synthesized.These quinones gave a stable radical kation and a stable radical anion on one-electron redox reactions showing an amphoteric property even though they do not contain any sulfur atom as an integral component.The radical cation and the radical anion of the tetra-t-butyl derivative have been characterized by EPR spectroscopy.