114574-46-8

Upstream product

• 70461-33-5 2-bromo-4,5-dimethoxybenzaldehyde dimethyl acetal 
• 120-14-9 3,4-dimethoxy-benzaldehyde 

Downstream Products

• 1025970-99-3 4-(3,4-Dimethoxy-phenyl)-9-hydroxy-6,7-dimethoxy-3H-naphtho[2,3-c]furan-1-one 
• 117671-62-2 4,5-dimethoxy-2-veratryl-benzoic acid 
• 16084-38-1 5,6-Dimethoxy-3-(3,4-dimethoxyphenyl)isobenzofuran-1(3H)-one 
• 104756-76-5 dimethyl 4-hydroxy-6,7-dimethoxy-1-(3',4'-dimethoxyphenyl)naphthalene-2,3-dicarboxylate 

Relevant academic research and scientific papers

A simple method for the synthesis of 4-aryl-9-oxynaphthofuranone lignans

The 9-aryl-4-oxynaphthofuran-1(3H)-one system is generally synthesized in two steps from α-aryl-o-toluic acid derivatives. The method involves a tandem conjugate addition-Dieckmann type condensation between α-lithiated α-aryl-o-toluic acid derivatives and

Arylnaphthalene lignans as novel series of hypolipidemic agents raising high-density lipoprotein level

A series of arylnaphthalene lignans were synthesized and tested for hypolipidemic activity. The most potent compound (4b) (TA-7552) not only reduced serum cholesterol, but also increased high-density lipoproteins cholesterol in rats. The effective dose of