15236-11-0

Basic information

• Product Name: 4',7-dimethoxyisoflavanone
• CAS NO: 15236-11-0
• Molecular Weight: 284.312
• Mol File: 15236-11-0.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: 4',7-dimethoxyisoflavanone(CAS DataBase Reference)
• NIST Chemistry Reference: 4',7-dimethoxyisoflavanone(15236-11-0)
• EPA Substance Registry System: 4',7-dimethoxyisoflavanone(15236-11-0)

Safety Data

• Hazardous Substances Data: 15236-11-0(Hazardous Substances Data)

Upstream product

• 96682-26-7 2-hydroxy-4-methoxyphenyl α-hydroxymethyl-4-methoxybenzyl ketone 
• 96682-33-6 3-hydroxymethyl-7-methoxy-3-(4'-methoxyphenyl)-2,3-dihydro-4H-1-benzopyran-4-one 
• 5720-07-0 4-methoxyphenylboronic acid 
• 73220-42-5 3-iodo-7-methoxy-chromen-4-one 
• 39604-64-3 1-(2-hydroxy-4-methoxyphenyl)-2-(4-methoxyphenyl)ethanone 
• 153488-87-0 3-allyloxycarbonyl-7-methoxychroman-4-one 
• 42327-52-6 7-methoxy-chroman-4-one 
• 18649-43-9 4-methoxyphenyllead(IV) triacetate 
• 51-80-9 bis-(dimethylamino)methane 
• 153488-96-1 3-allyloxycarbonyl-7-methoxy-3-(4-methoxyphenyl)chroman-4-one 
• 75-11-6 diiodomethane 
• 15236-11-0 (S)-7-methoxy-3-(4-methoxy-phenyl)-chroman-4-one 
• 4366-35-2 4',7-dimethoxyisoflavan 
• 1157-39-7 7-methoxy-3-(4-methoxyphenyl)-4H-chromen-4-one 

Downstream Products

• 15236-11-0 4',7-dimethoxyisoflavanone 
• 97080-01-8 4-ethyl-7-methoxy-3-(4-methoxy-phenyl)-2H-chromene 
• 93877-74-8 7-methoxy-3-(4-methoxy-phenyl)-4-methyl-2H-chromene 
• 95431-45-1 7-Methoxy-3-(4-methoxy-phenyl)-4-phenyl-chroman-4-ol 
• 96309-20-5 7-methoxy-3-(4-methoxy-phenyl)-4-phenyl-2H-chromene 
• 4366-35-2 4',7-dimethoxyisoflavan 
• 4281-32-7 (3R,4R)-7-methoxy-3-(4-methoxyphenyl)chroman-4-ol 
• 4281-32-7 cis-4,7'-Dimethoxy-isoflavan-4-ol 
• 4308-53-6 7-methoxy-3-(4-methoxyphenyl)-2H-chromene 
• 50-00-0 formaldehyd 
• 39604-64-3 1-(2-hydroxy-4-methoxyphenyl)-2-(4-methoxyphenyl)ethanone 
• 1157-39-7 7-methoxy-3-(4-methoxyphenyl)-4H-chromen-4-one 
• 20921-26-0 7-Methoxy-3-(4-methoxy-phenyl)-chroman-4-one oxime 

Relevant articles and documents

Enantioselective Synthesis of Isoflavanones by Catalytic Dynamic Kinetic Resolution

A ruthenium-catalyzed asymmetric transfer hydrogenation of racemic isoflavanones with dynamic kinetic resolution yields virtually enantiopure isoflavanols as single diastereomers. Subsequent oxidation gives rise to isoflavanones in high enantiomeric purit

A simple one-pot synthesis of isoflavanones

A new simple one-pot synthesis of isoflavanones 2 by reaction of benzyl 2-hydroxyphenylketones 1 with bis(dimethylamino)methane in boiling ethanol is described.

Synthesis of isoflavanones from isoflavones by reduction with sodium hydrogen telluride

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