49619-88-7

Basic information

• Product Name: 2-{4-[5-(5,7-dimethoxy-4-oxo-4H-chromen-2-yl)-2-methoxyphenoxy]phenyl}-5,7-dimethoxy-4H-chromen-4-one
• CAS NO: 49619-88-7
• Molecular Formula: C₃₅H₂₈O₁₀
• Molecular Weight: 608.5908
• Mol File: 49619-88-7.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 805.1°C at 760 mmHg
• Flash Point: 245.5°C
• Density: 1.323g/cm³
• Vapor Pressure: 5.86E-26mmHg at 25°C
• Refractive Index: 1.622
• CAS DataBase Reference: 2-{4-[5-(5,7-dimethoxy-4-oxo-4H-chromen-2-yl)-2-methoxyphenoxy]phenyl}-5,7-dimethoxy-4H-chromen-4-one(CAS DataBase Reference)
• NIST Chemistry Reference: 2-{4-[5-(5,7-dimethoxy-4-oxo-4H-chromen-2-yl)-2-methoxyphenoxy]phenyl}-5,7-dimethoxy-4H-chromen-4-one(49619-88-7)
• EPA Substance Registry System: 2-{4-[5-(5,7-dimethoxy-4-oxo-4H-chromen-2-yl)-2-methoxyphenoxy]phenyl}-5,7-dimethoxy-4H-chromen-4-one(49619-88-7)

Safety Data

• Hazardous Substances Data: 49619-88-7(Hazardous Substances Data)

Usage

Family

Chromenones

Composition

Functional Groups:
Methoxy
Carbonyl
Phenyl
Core Structure: Chromenone

Biological Activities

Antioxidant
Anti-inflammatory
Anticancer

Potential Applications

Drug candidate for various therapeutic purposes

Research Status

Ongoing research and development in pharmaceutical and biomedical fields.

Upstream product

• 2748-98-3 3-(4-formylphenoxy)-4-methoxybenzaldehyde 
• 621-59-0 isovanillin 
• 459-57-4 4-fluorobenzaldehyde 
• 33554-52-8 3′-hydroxy-5,7,4′-trimethoxyflavone 
• 90-24-4 2-hydroxy-4,6-dimethoxyacetophenone 
• 1122-91-4 4-bromo-benzaldehyde 
• 104-88-1 4-chlorobenzaldehyde 
• 76554-31-9 3-(4-chlorophenyl)-1-(2-hydroxy-4,6-dimethoxyphenyl)prop-2-en-1-one 
• 720676-01-7 2-hydroxy-4,6-dimethoxy-4'-fluorochalcone 
• 38186-71-9 2′,3-dihydroxy-4,4′,6′-trimethoxychalcone 

Downstream Products

• 50276-96-5 Ochnaflavone 

Relevant articles and documents

Synthesis of ochnaflavone and its inhibitory activity on PGE2 production

Ochnaflavone, a naturally occurring biflavonoid composed of two units of apigenin (5,7,4′-trihydroxyflavone) joined via a C-O-C linkage, was first synthesized and evaluated its inhibitory activity on PGE2 production. Total synthesis was accompl