10496-69-2

Basic information

• Product Name: 2-(3,4-Dimethoxyphenyl)-3,4-dihydro-5,7-dimethoxy-2H-1-benzopyran-4-ol
• Synonyms: 2-(3,4-Dimethoxyphenyl)-3,4-dihydro-5,7-dimethoxy-2H-1-benzopyran-4-ol
• CAS NO: 10496-69-2
• Molecular Formula: C₁₉H₂₂O₆
• Molecular Weight: 0
• Mol File: 10496-69-2.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-(3,4-Dimethoxyphenyl)-3,4-dihydro-5,7-dimethoxy-2H-1-benzopyran-4-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(3,4-Dimethoxyphenyl)-3,4-dihydro-5,7-dimethoxy-2H-1-benzopyran-4-ol(10496-69-2)
• EPA Substance Registry System: 2-(3,4-Dimethoxyphenyl)-3,4-dihydro-5,7-dimethoxy-2H-1-benzopyran-4-ol(10496-69-2)

Safety Data

• Hazardous Substances Data: 10496-69-2(Hazardous Substances Data)

Usage

Structure

Benzopyran ring, multiple methoxy groups, and a phenyl group
The compound's complex structure consists of a benzopyran ring (a type of heterocyclic organic compound), several methoxy groups (an oxygen atom bonded to a methyl group), and a phenyl group (a carbon-based ring structure).

Classification

Flavonoid derivative
This compound is a derivative of flavonoids, a class of natural compounds found in various plants.

Properties

Antioxidant and anti-inflammatory
Flavonoids, including this specific compound, are known for their potential antioxidant and anti-inflammatory properties, which can help protect cells from damage and reduce inflammation.

Therapeutic potential

Possible benefits due to structural similarity to other flavonoids
The compound's structural similarity to other flavonoids suggests that it may have potential therapeutic benefits, although further research is needed to confirm this.

Ongoing research

Biological activities and potential medicinal properties
Scientists are currently investigating the biological activities of this compound and its potential medicinal properties, as its unique structure and potential benefits make it an interesting target for scientific study.

Upstream product

• 10496-69-2 5,7,3',4'-tetramethoxyflavan-4β-ol 
• 88363-06-8 4α-acetoxy-5,7,3',4'-trimethoxyflavan 
• 17060-20-7 2,3-dihydro-5,7-dimethoxy-2-(4'-dimethoxyphenyl)-4H-1-benzopyran-4-one 
• 88363-06-8 4β-acetoxy-5,7,3',4'-trimethoxyflavan 
• 67-56-1 methanol 

Downstream Products

• 88363-06-8 4α-acetoxy-5,7,3',4'-trimethoxyflavan 
• 88363-06-8 4β-acetoxy-5,7,3',4'-trimethoxyflavan 
• 10496-69-2 5,7,3',4'-pentamethoxyflavan-4α-ol 
• 88363-07-9 4α,5,7,3',4'-pentamethoxyflavan 
• 88363-07-9 4β,5,7,3',4'-pentamethoxyflavan 

Relevant articles and documents

Epimerisation of 4-Acetoxyflavans and Flavan-4-ols

5,7,3',4'-Tetramethoxyflavan-4β-ol reacts at 0 deg C with pyridine, ang a trace of acetic acid to give the 4β-acetoxy derivative but at 90 deg C the 4α-acetoxyflavan is formed.Either acetate when equilibrated with this acetylating agent yields a mixture o