67858-30-4

Basic information

• Product Name: 2-(3,4,5-TriMethoxyphenyl)-4H-chroMen-4-one
• Synonyms: 2-(3,4,5-TriMethoxyphenyl)-4H-chroMen-4-one;2-(3,4,5-TriMethoxyphenyl)chroMen-4-one;3‘,4‘,5‘-Trimethoxyavone
• CAS NO: 67858-30-4
• Molecular Formula: C₁₈H₁₆O₅
• Molecular Weight: 312.31664
• Mol File: 67858-30-4.mol
• Article Data: 35

Chemical Properties

• Boiling Point: 458.3°Cat760mmHg
• Flash Point: 203°C
• Appearance: /
• Density: 1.242g/cm³
• Vapor Pressure: 1.39E-08mmHg at 25°C
• Refractive Index: 1.585
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 2-(3,4,5-TriMethoxyphenyl)-4H-chroMen-4-one(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(3,4,5-TriMethoxyphenyl)-4H-chroMen-4-one(67858-30-4)
• EPA Substance Registry System: 2-(3,4,5-TriMethoxyphenyl)-4H-chroMen-4-one(67858-30-4)

Safety Data

• Hazardous Substances Data: 67858-30-4(Hazardous Substances Data)

Usage

General Description

2-(3,4,5-Trimethoxyphenyl)-4H-chromen-4-one, also known as norwogonin, is a chemical compound found in various plants such as the soybean and licorice. It is a member of the flavonoid family and has been reported to possess antioxidant, anti-inflammatory, and anticancer properties. 2-(3,4,5-TriMethoxyphenyl)-4H-chroMen-4-one has been the subject of various studies for its potential therapeutic effects on conditions such as diabetes, cardiovascular diseases, and neurodegenerative disorders. Its unique chemical structure and bioactive properties make it a promising candidate for further research and potential development of pharmaceutical applications.

InChI:InChI=1/C18H16O5/c1-20-16-8-11(9-17(21-2)18(16)22-3)15-10-13(19)12-6-4-5-7-14(12)23-15/h4-10H,1-3H3

Upstream product

• 67858-32-6 1-(2-hydroxyphenyl)-3-(3,4,5-trimethoxyphenyl)propane-1,3-dione 
• 126432-36-8 2-(3′,4′,5′-trihydroxyphenyl)chromen-4-one (3′,4′,5′-trihydroxyflavone) 
• 77-78-1 dimethyl sulfate 
• 67-56-1 methanol 
• 132018-03-2 3-(methoxycarbonyl)-2-(3,4,5-trimethoxyphenyl)-4H-benzopyran-4-one 
• 136003-89-9 1-[2-(tert-Butyl-dimethyl-silanyloxy)-phenyl]-3-(3,4,5-trimethoxy-phenyl)-propane-1,3-dione 
• 59817-22-0 (2E)-1-(2-hydroxyphenyl)-3-(3,4,5-trimethoxyphenyl)prop-2-en-1-one 
• 125130-99-6 3-(2-hydroxyphenyl)-3',4',5'-trimethoxyprop-2-ynophenone 
• 5720-07-0 4-methoxyphenylboronic acid 
• 454482-66-7 3-bromo-2-(3,4,5-trimethoxyphenyl)-4H-chromen-4-one 
• 13139-86-1 4-methoxyphenyl magnesium bromide 
• 533-58-4 2-Iodophenol 
• 155721-23-6 5-(2-hydroxyphenyl)-3-(3,4,5-trimethoxyphenyl)isoxazole 
• 5101-44-0 2-ethynyl-phenol 

Downstream Products

• 454482-66-7 3-bromo-2-(3,4,5-trimethoxyphenyl)-4H-chromen-4-one 
• 1370734-41-0 ethyl 2?(4?oxo?2?(3,4,5?trimethoxyphenyl)?4H?chromen?3?yl)acetate 
• 1370734-47-6 3-(2-(4-chlorophenyl)-2-oxoethyl)-2-(3,4,5-trimethoxyphenyl)-4H-chromen-4-one 
• 1370734-52-3 3-(2-(biphenyl-4-yl)-2-oxoethyl)-2-(3,4,5-trimethoxyphenyl)-4H-chromen-4-one 
• 126432-36-8 2-(3′,4′,5′-trihydroxyphenyl)chromen-4-one (3′,4′,5′-trihydroxyflavone) 
• 155721-23-6 5-(2-hydroxyphenyl)-3-(3,4,5-trimethoxyphenyl)isoxazole 
• 143468-23-9 3-Nitro-2-(3,4,5-trimethoxy-phenyl)-chromen-4-one 

Relevant articles and documents

Divergent synthesis of flavones and flavanones from 2′-hydroxydihydrochalconesviapalladium(ii)-catalyzed oxidative cyclization

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Synthesis, biological evaluation, and NMR studies of 3-fluorinated derivatives of 3′,4′,5′-trihydroxyflavone and 3′,4′,5′-trimethoxyflavone

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