174876-47-2

Upstream product

• 174876-42-7 3,4-ethylenedioxy-3',4'-dimethoxydeoxybenzoin 
• 493-09-4 benzo-1,4-dioxane 
• 93-40-3 (3,4-Dimethoxyphenyl)acetic acid 
• 174876-44-9 2-[2-(3,5-Di-tert-butyl-4-hydroxy-benzyl)-4,5-dimethoxy-phenyl]-1-(2,3-dihydro-benzo[1,4]dioxin-6-yl)-ethanone 

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.