2178-51-0

Usage

Uses

There is no information provided on the specific uses of 2,5-Cyclohexadien-1-one, 4-[3,5-bis(1-methylethyl)-4-oxo-2,5-cyclohexadien-1-ylidene]-2,6-bis(1-methylethyl)-. However, given its complex molecular structure and potential reactivity, it may have potential applications in various industries, such as pharmaceuticals, materials science, or chemical research. Further analysis and research would be required to determine its specific uses and potential hazards.

Upstream product

• 2078-54-8 2,6-diisopropylphenol 
• 2416-95-7 3,3',5,5'-tetraisopropyl-[1,1'-biphenyl]-4,4'-diol 

Downstream Products

• 2416-95-7 3,3',5,5'-tetraisopropyl-[1,1'-biphenyl]-4,4'-diol 
• 1988-11-0 2,6-diisopropyl-1,4-benzoquinone 

Relevant academic research and scientific papers

Solubilization of dipropofol, an antibacterial agent, using saccharide and ascorbic acid

Dipropofol has a strong antibacterial activity against Gram-positive bacteria. However, it lacked the solubility in water and this property was supposed to limit its efficacy. We tried to improve the solubility and found a new solubilization method of dipropofol in water by the addition of a monosaccharide or ascorbic acid.

A green mesostructured vanadosilicate catalyst and its unprecedented catalytic activity for the selective synthesis of 2,6-disubstituted p-benzoquinones

We have developed a green method for the production of 2,6-disubstituted p-benzoquinones (DSBQs) by liquid-phase oxidations of di/tri-substituted phenols using two-dimensional hexagonally thick-walled mesoporous vanadosilicate catalysts. In particular, 2,6-di-tert-butyl-p-benzoquinone was synthesized by the oxidation of 2,6-di-tert-butylphenol, using various reaction parameters, over mesoporous VSBA-15 catalysts synthesized with various vanadium contents. A promising chemical treatment method for the preparation of green mesoporous VSBA-15(5) or W-VSBA-15(5) (W: washed) catalysts was successfully used in the presence of ammonium acetate solution to remove moderately toxic non-framework V2O5 crystallite species from the active surface, and the catalytic activity of the recovered green mesoporous VSBA-15(5) catalyst was determined. To confirm the green aspects, recyclability and hot-catalytic filtration experiments were performed. The combined results show that the green mesoporous VSBA-15(5) is a highly active, recyclable, and promising heterogeneous catalyst for the selective synthesis of DSBQs (98-100%), and has unprecedented catalytic activity compared with other mesoporous vanadosilicate catalysts. The Royal Society of Chemistry 2014.

Oxidative coupling of some 2,6-disubstituted phenol derivatives in perchloric acid mediated by cerium(IV) ions

2,6-Disubstituted phenol derivatives have been oxidized by cerium(IV) perchlorate in aqueous or aqueous-acetonitrile solutions of perchloric acid as well as in two-phase systems to the corresponding 1,4-benzoquinones, 4,4′-diphenoquinones, and oligomeric

Choice of Manganese(III) Complexes for the Synthesis of 4,4'-Biphenyldiols and 4,4'-Diphenoquinones

2,6-Disubstituted phenols are oxidized with tris(2,4-pentanedionato)manganese(III), , in glacial acetic acid to give the corresponding 4,4'-biphenyldiols in high yields, whereas similar reactions using manganase(III) acetate, , instead of quantitatively yield the corresponding 4,4'-diphenoquinones.Cross-coupling reactions of 2,6-di-t-butylphenol and other substituted phenols afford the corresponding cross-coupled 4,4'-biphenyldiols and 4,4'-diphenoquinones together with oxidation products derived from them starting phenols themselves.The advantageous use of and Mn(OAc)3> in the ubiqitous phenol coupling reaction is discussed.

Mushroom tyrosinase catalysed coupling of hindered phenols: A novel approach for the synthesis of diphenoquinones and bisphenols

An efficient oxidative carbon-carbon coupling of hindered phenols leading to diphenoquinones and bisphenols by mushroom tyrosinase is reported.