80140-28-9

Upstream product

• 3162-28-5 2-hydroxy-3,4,5,6-tetramethoxyacetophenone 
• 1486-54-0 3,4-dibenzyloxybenzoyl chloride 
• 14786-40-4 1-(2,3,4,5,6-pentamethoxyphenyl)ethan-1-one 
• 91556-09-1 2,3,4,5,6-pentamethoxybenzoic acid 
• 92157-76-1 methyl 2,3,4,5,6-pentamethoxybenzoate 
• 7169-08-6 2,3,4,5,6-Pentamethoxy-benzoylchlorid 

Downstream Products

• 80140-29-0 2-Hydroxy-3',4'-dibenzyloxy-3,4,5,6-tetramethoxydibenzoylmethane 
• 70360-12-2 2-(3,4-dihydroxy-phenyl)-5-hydroxy-6,7,8-trimethoxy-chromen-4-one 
• 80140-31-4 3',4'-dihydroxy-5,6,7,8,-tetramethoxyflavone 
• 80140-30-3 3',4'-Dibenzyloxy-5,6,7,8-tetramethoxyflavone 
• 80140-32-5 Acetic acid 2-(3,4-diacetoxy-phenyl)-6,7,8-trimethoxy-4-oxo-4H-chromen-5-yl ester 

Relevant academic research and scientific papers

Nobiletin metabolites: Synthesis and inhibitory activity against matrix metalloproteinase-9 production

A divergent synthesis of nobiletin metabolites was developed through highly oxygenated acetophenone derivative. We used commercially available methyl 3,4,5-trimethoxybenzoate as a starting material for concise preparation of the key intermediate, 2′-hydro

Synthesis of 5,3',4'-Trihydroxy-6,7,8-trimethoxyflavone

The structure of a new trihydroxytrimethoxyflavone, isolated from Sideritis leucantha, as 5,3',4'-trihydroxy-6,7,8-trimethoxyflavone (I) has now been confirmed by its synthesis. 2-(3',4'-Dibenzyloxy)benzoyloxy-3,4,5,6-tetramethoxyacetophenone (VI) on Bake