7249-35-6

Basic information

• Product Name: 2-(4-acetyl-2-methoxyphenoxy)-1-(3,4-dimethoxyphenyl)ethanone
• CAS NO: 7249-35-6
• Molecular Formula: C₁₉H₂₀O₆
• Molecular Weight: 344.3585
• Mol File: 7249-35-6.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 524.8°C at 760 mmHg
• Flash Point: 231°C
• Density: 1.175g/cm³
• Vapor Pressure: 4.17E-11mmHg at 25°C
• Refractive Index: 1.544
• CAS DataBase Reference: 2-(4-acetyl-2-methoxyphenoxy)-1-(3,4-dimethoxyphenyl)ethanone(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-acetyl-2-methoxyphenoxy)-1-(3,4-dimethoxyphenyl)ethanone(7249-35-6)
• EPA Substance Registry System: 2-(4-acetyl-2-methoxyphenoxy)-1-(3,4-dimethoxyphenyl)ethanone(7249-35-6)

Safety Data

• Hazardous Substances Data: 7249-35-6(Hazardous Substances Data)

Usage

Molecular weight

287.34 g/mol

Functional groups

ketone, aryl ether, acetyl, methoxy

Aromatic ring structures

two

Usage

organic synthesis, pharmaceutical research

Potential applications

development of new drugs, pharmaceutical products, cosmetics, material science

Additional research needed

properties, potential uses

Upstream product

• 1835-02-5 2-Bromo-1-(3,4-dimethoxyphenyl)ethanone 
• 498-02-2 1-(3-methoxy-4-hydroxyphenyl)ethanone 

Relevant articles and documents

Cation Radical Accelerated Nucleophilic Aromatic Substitution via Organic Photoredox Catalysis

Nucleophilic aromatic substitution (SNAr) is a direct method for arene functionalization; however, it can be hampered by low reactivity of arene substrates and their availability. Herein we describe a cation radical-accelerated nucleophilic aromatic substitution using methoxy- and benzyloxy-groups as nucleofuges. In particular, lignin-derived aromatics containing guaiacol and veratrole motifs were competent substrates for functionalization. We also demonstrate an example of site-selective substitutive oxygenation with trifluoroethanol to afford the desired trifluoromethylaryl ether.