76672-90-7

Upstream product

• 57601-14-6 2'-hydroxy-3,4,4'-trimethoxychalcone 
• 120-14-9 3,4-dimethoxy-benzaldehyde 
• 552-41-0 1-(2-hydroxy-4-methoxyphenyl)ethanone 

Downstream Products

• 76672-92-9 3-(3,4-dimethoxybenzyl)-7-methoxy-4-chromanone 
• 76672-91-8 3,4,4',3''',4'',4'''-Hexamethoxy-2',2'''-bi(dihydro-chalkonyloxy)methane 
• 10493-09-1 7,3',4'-trimethoxyflavanone 
• 22395-24-0 3',4',7-trimethoxyflavone 
• 111254-23-0 (3R,4S)-3,4-dihydroxy-3-(3,4-dimethoxybenzyl)-7-methoxychroman 
• 113122-58-0 (R)-(-)-O-trimethylsappanone B 
• 91100-83-3 3-(3,4-dimethoxybenzyl)-7-methoxy-4H-chromen-4-one 
• 105245-59-8 2'-Hydroxy-3,4,4'-trimethoxy-α-hydroxymethyldihydrochalcone 

Relevant academic research and scientific papers

Synthesis and biological evaluation of chalcone, dihydrochalcone, and 1,3-diarylpropane analogs as anti-inflammatory agents

Twenty-one chalcones were prepared via aldol condensation and subsequent reduction of these compound led to the corresponding dihydrochalcone and 1,3-diphenylpropane derivatives. The synthetic products were examined for their effects on NO inhibition in L

Facile reduction of chalcones to dihydrochalcones with NaBH4/Ni2+ system

Chalcones have been found to undergo facile reduction on treatment with sodium borohydride-nickel chloride system in dioxan-methanol medium to afford dihydrochalcones.

A New Biogenetic Approach for the Synthesis of Homoisoflavanones

2'-Hydroxydihydrochalkones on refluxing with methylene iodide in acetone medium in the presence of anhydrous potassium carbonate have been found to yield bi(dihydrochalkonyloxy)methanes and homoisoflavanones.