34086-51-6

Basic information

• Product Name: 4',7-Dimethoxy-5-hydroxyisoflavone
• Synonyms: BIOCHANIN A METHYL ETHER;BIOCHANIN A-7-METHYL ETHER;GENISTEIN-4',7-DIMETHYL ETHER;GENISTEIN-7,4'-DIMETHYL ETHER;4',7-DIMETHOXY-5-HYDROXYISOFLAVONE;5-HYDROXY-7-METHOXY-3-(4-METHOXY-PHENYL)-CHROMEN-4-ONE;7,4'-DIMETHOXY-5-HYDROXYISOFLAVONE;5HYDROXY47DIMETHOXYISOFLAVONE
• CAS NO: 34086-51-6
• Molecular Formula: C₁₇H₁₄O₅
• Molecular Weight: 298.29
• Product Categories: Iso-Flavones
• Mol File: 34086-51-6.mol
• Article Data: 8

Chemical Properties

• Melting Point: 140～142℃
• Boiling Point: 515.2 °C at 760 mmHg
• Flash Point: 193.3 °C
• Appearance: /
• Density: 1.321 g/cm³
• PKA: 6.33±0.20(Predicted)
• CAS DataBase Reference: 4',7-Dimethoxy-5-hydroxyisoflavone(CAS DataBase Reference)
• NIST Chemistry Reference: 4',7-Dimethoxy-5-hydroxyisoflavone(34086-51-6)
• EPA Substance Registry System: 4',7-Dimethoxy-5-hydroxyisoflavone(34086-51-6)

Safety Data

• WGK Germany: 3
• F: 10
• Hazardous Substances Data: 34086-51-6(Hazardous Substances Data)

Usage

General Description

4',7-Dimethoxy-5-hydroxyisoflavone is a chemical compound with potent antioxidant and anti-inflammatory properties. It belongs to the isoflavone class of compounds, which are found naturally in plants and have been researched for their potential health benefits. This specific compound has been studied for its ability to protect cells from oxidative damage and reduce inflammation, making it a potential candidate for the development of new therapeutic agents for various diseases. Additionally, it has been shown to have potential anticancer properties and may help in the prevention and treatment of certain types of cancer. Further research is needed to fully understand the mechanisms and potential uses of 4',7-Dimethoxy-5-hydroxyisoflavone in medicine and health.

Upstream product

• 552-59-0 prunetin 
• 67-64-1 acetone 
• 77-78-1 dimethyl sulfate 
• 74-88-4 methyl iodide 
• 491-80-5 5,7-Dihydroxy-3-(4-methoxy-phenyl)-chromen-4-on 
• 446-72-0 5,7-Dihydroxy-3-(4-hydroxy-phenyl)-chromen-4-on 
• 152-95-4 sophoricoside 
• 1162-82-9 4',5,7-trimethoxyisoflavone 
• 186581-53-3 diazomethane 
• 64-17-5 ethanol 

Downstream Products

• 111066-96-7 5-acetoxy-7-methoxy-3-(4-methoxy-phenyl)-chromen-4-one 
• 104-01-8 4-Methoxyphenylacetic acid 
• 2174-64-3 5-methoxyresorcinol 
• 1179998-23-2 2-(2,6-dihydroxy-4-methoxyphenyl)-3-(4-methoxyphenyl)-pyrimido[1,2-a]benzimidazole 
• 1108742-47-7 2-amino-4-(2,6-dihydroxy-4-methoxyphenyl)-5-(4-methoxyphenyl)pyrimidine 
• 1427272-61-4 3-cyano-6-(4-methoxy-2,6-dihydroxyphenyl)-5-(4-methoxyphenyl)pyridine-2(1H)-thione 
• 1456626-72-4 3-cyano-6-(4-methoxy-2,6-dihydroxyphenyl)-5-(4-methoxyphenyl)pyridin-2(1H)-one 
• 1606136-79-1 2-methyl-6-(4-methoxyphenyl)-7-(2,6-dihydroxyl-4-methoxyphenyl)pyrazolo[1,5-a]pyrimidine 

Relevant articles and documents

Hydrogen bonding and π-π stacking in dimethylgenistein

The title compound, 5-hydroxy-4′,7-dimethoxyisoflavone, Q 17H14O5, is composed of a benzopyranone moiety, a phenyl moiety and two methoxy groups. The benzopyranone ring is not coplanar with the phenyl ring, the dihedral an

Application of Mannich bases to the synthesis of hydroxymethylated isoflavonoids as potential antineoplastic agents

The regiospecific Mannich aminomethylation of 7-hydroxyisoflavonoids using bis(N,N-dimethylamino)methane afforded C-8 substituted N,N-dimethylaminomethyl adducts, and the regioselective aminomethylation of 5-hydroxy-7-methoxyisoflavonoids afforded predomi

Biotransformation of isoflavones by the larvae of the common cutworm (Spodoptera litura)

Biotransformation of the 5,7,4′-trimethoxyisoflavone (1), 6,7,4′-trimethoxyisoflavone (2), and 7,4′-dimethoxyisoflavone (3) by insects, Spodoptera litura was investigated. Compound 1 was transformed to 5-hydroxy-7,4′-dimethoxyisoflavone (4), 7-hydroxy-5,4