74693-73-5

Basic information

• Product Name: 6,7-dihydroxy-3',4'-dimethoxyisoflavone
• CAS NO: 74693-73-5
• Molecular Weight: 314.295
• Mol File: 74693-73-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 6,7-dihydroxy-3',4'-dimethoxyisoflavone(CAS DataBase Reference)
• NIST Chemistry Reference: 6,7-dihydroxy-3',4'-dimethoxyisoflavone(74693-73-5)
• EPA Substance Registry System: 6,7-dihydroxy-3',4'-dimethoxyisoflavone(74693-73-5)

Safety Data

• Hazardous Substances Data: 74693-73-5(Hazardous Substances Data)

Upstream product

• 66116-74-3 1-(2,4,5-trihydroxyphenyl)-2-(3,4-dimethoxyphenyl)ethanone 
• 68-12-2 N,N-dimethyl-formamide 
• 533-73-3 1,2,4-Trihydroxybenzene 
• 93-17-4 3,4-dimethoxyphenylacetonitrile 
• 74693-71-3 2',4',5'-tribenzyloxy-3,4-dimethoxychalkone 
• 74693-70-2 2'-hydroxy-4',5'-dibenzyloxy-3,4-dimethoxychalkone 
• 74693-72-4 2',4',5'-tribenzyloxy-3,4-dimethoxychalkone epoxide 
• 93435-58-6 1-(2,3,4-trihydroxyphenyl)-2-(3',4'-dimethoxyphenyl)ethanone 
• 124-63-0 methanesulfonyl chloride 

Downstream Products

• 61243-76-3 6,7-methylenedioxy-3',4'-dimethoxyisoflavone 

Relevant articles and documents

Isoflavans derivatives as inhibitors of soybean lipoxygenase: In-vitro and docking studies

The lipoxygenases (LOX) are a family of non-heme iron-containing dioxygenases which catalyze the stereospecific insertion of molecular oxygen into arachidonic acid, leading to hydroxy derivatives as end products. In this work, we studied the behavior of s

A Convenient Synthesis of 6,7-Methylenedioxy-3',4'-dimethoxyisoflavone

6,7-Methylenedioxy-3',4'-dimethoxyisoflavone (I) has been synthesized from 2',4',5'-tribenzyloxy-3,4-dimethoxy-chalkone (III).The epoxide (IV) of III is converted into the isoflavone (VI) trough the α-formyldesoxybenzoin (V).Methylenation of VI gives I.