174876-44-9

Upstream product

• 493-09-4 benzo-1,4-dioxane 
• 93-40-3 (3,4-Dimethoxyphenyl)acetic acid 
• 88-26-6 3,5-di-tert-butyl-4-hydroxybenzyl alcohol 
• 174876-42-7 3,4-ethylenedioxy-3',4'-dimethoxydeoxybenzoin 

Downstream Products

• 174876-47-2 2,6-Di-tert-butyl-4-{2-[2-(2,3-dihydro-benzo[1,4]dioxin-6-yl)-2-oxo-ethyl]-4,5-dimethoxy-benzylidene}-cyclohexa-2,5-dienone 

Relevant academic research and scientific papers

Sterically Hindered 1,4-Methylenebenzoquinones in the Synthesis of Six-Membered N-, O-, S-, and Se-Heterocycles

In the presence of acids or bases or on heating 2,6-di-tert-butyl-4-(4,5-dimethoxy-2-phenacylbenzylidene)-2,5-cyclohexadien-1-ones are converted into isochromenes; treatment with hydroxylamine yields isoquinoline derivatives possessing high antioxidant activity.Reactions of these methylenebenzoquinones with elemental sulfur and selenium result in formation of 1,2-dihydro-2-thia(selena)naphthalene 2-oxides.