109250-67-1

Upstream product

• 93-40-3 (3,4-Dimethoxyphenyl)acetic acid 
• 151-10-0 1,3-Dimethoxybenzene 

Downstream Products

• 121816-47-5 2-(2,4-dimethoxy-phenyl)-3-(3,4-dimethoxy-phenyl)-7-hydroxy-chromenylium; picrate 
• 304850-42-8 1-(2,4-dimethoxyphenyl)-2-(3',4'-dimethoxyphenyl)-1-oxo-3-ethoxy-propane 
• 119276-13-0 2-(2,4-dimethoxy-phenyl)-3-(3,4-dimethoxy-phenyl)-7-hydroxy-6-methoxy-chromenylium; chloride 
• 102750-10-7 2-(2,4-dimethoxy-phenyl)-3-(3,4-dimethoxy-phenyl)-quinoxaline 
• 349407-99-4 (3,4-dimethoxy-phenyl)-acetic acid-(2,4-dimethoxy-anilide) 
• 102948-62-9 2-(2,4-dimethoxy-phenyl)-3-(3,4-dimethoxy-phenyl)-6-methoxy-chromen-7-one 
• 109469-76-3 2,4,3',4'-Tetramethoxy-benzil 

Relevant academic research and scientific papers

ARYL DI-SUBSTITUTED PROPENONE COMPOUNDS

Compounds of formula (I): wherein R1 and R4 are OR7, R2 and R3 are H or OR7, with the proviso that when R2 is OR7 then R3 is H, and when R3 is OR7 then Rsu

Isoflavone metabolites

There are disclosed compounds of formulae (I) or (II) in which A is selected from the group consisting of (1), (2), (3) and (4);OH, and one of R1 and R2 is selected from H, OH and OCH3, and the other of R1 and R

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.