39604-65-4

Upstream product

• 93434-89-0 1-(2,4-dihydroxy-3-methylphenyl)-2-(4-methoxyphenyl)ethanone 
• 77-78-1 dimethyl sulfate 
• 74-88-4 methyl iodide 
• 104-01-8 4-Methoxyphenylacetic acid 
• 104-47-2 p-methoxybenzylnitrile 
• 608-25-3 2-methylbenzene-1,3-diol 

Downstream Products

• 1571899-94-9 7-methoxy-3-(4-methoxyphenyl)-3',4'-dimethoxyflavone-8-acetic acid 
• 1571899-93-8 7-methoxy-3-(4-methoxyphenyl)-4'-methoxyflavone-8-acetic acid 
• 1571899-92-7 7-methoxy-3-(4-methoxyphenyl)-flavone-8-acetic acid 
• 1571900-05-4 2-(3,4-dimethoxyphenyl)-7-methoxy-3-(4-methoxyphenyl)-8-methyl-4H-chromen-4-one 
• 1571900-03-2 7-methoxy-2,3-bis(4-methoxyphenyl)-8-methyl-4H-chromen-4-one 
• 1571900-02-1 7-methoxy-3-(4-methoxyphenyl)-8-methyl-2-phenyl-4H-chromen-4-one 
• 860369-03-5 4',7-dimethoxy-8-methylisoflavone 
• 288266-76-2 7-acetoxy-3-(4-acetoxy-phenyl)-8-methyl-chromen-4-one 
• 139256-08-9 7-hydroxy-3-(4-hydroxyphenyl)-8-methyl-4H-chromen-4-one 

Relevant academic research and scientific papers

Synthesis, selective cytotoxicities and probable mechanism of action of 7-methoxy-3-arylflavone-8-acetic acids

Thirteen new analogues of flavone-8-acetic acid, that is, compounds 10a-m bearing a methoxy group at the 7-position and diverse subsitiuents on the benzene ring at the 2- and 3-positions of flavone nucleus, were synthesized and evaluated for their direct