38209-58-4

Basic information

• Product Name: 3,4-Dimethoxy-α-oxobenzeneacetic acid methyl ester
• Synonyms: 3,4-Dimethoxy-α-oxobenzeneacetic acid methyl ester;Methyl 2-(3,4-diMethoxyphenyl)-2-oxoacetate
• CAS NO: 38209-58-4
• Molecular Formula: C₁₁H₁₂O₅
• Molecular Weight: 238.238
• Mol File: 38209-58-4.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 341.8°C at 760 mmHg
• Flash Point: 151.3°C
• Appearance: /
• Density: 1.186g/cm³
• Vapor Pressure: 7.88E-05mmHg at 25°C
• Refractive Index: 1.505
• CAS DataBase Reference: 3,4-Dimethoxy-α-oxobenzeneacetic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 3,4-Dimethoxy-α-oxobenzeneacetic acid methyl ester(38209-58-4)
• EPA Substance Registry System: 3,4-Dimethoxy-α-oxobenzeneacetic acid methyl ester(38209-58-4)

Safety Data

• Hazardous Substances Data: 38209-58-4(Hazardous Substances Data)

Usage

InChI:InChI=1/C11H12O5/c1-14-8-5-4-7(6-9(8)15-2)10(12)11(13)16-3/h4-6H,1-3H3

Upstream product

• 5781-53-3 monomethyl oxalyl chloride 
• 91-16-7 1,2-dimethoxybenzene 
• 22675-96-3 2-methoxyphenoxy-3',4'-dimethoxyacetophenone 
• 140455-40-9 1-(3,4-dimethoxyphenyl)-2-phenoxy-1-ethanone 
• 67-56-1 methanol 
• 183303-74-4 1-(3,4-dimethoxyphenyl)-2-phenoxy-1-ethanol 
• 63987-72-4 2,2-dibromo-1-(3,4-dimethoxyphenyl)ethan-1-one 
• 1131-62-0 1-(3,4-dimethoxyphenyl)ethanone 
• 4732-70-1 3,4-dimethoxyphenylglyoxylic acid 
• 93-40-3 (3,4-Dimethoxyphenyl)acetic acid 
• 15964-79-1 methyl (3,4-dimethoxyphenyl)acetate 

Downstream Products

• 850794-62-6 2-(3,4-dimethoxyphenyl)-3-phenoxy-2-hydroxypropanoic acid 
• 850794-59-1 methyl 2-(3,4-dimethoxyphenyl)-3-phenoxy-2-hydroxypropanoate 
• 4732-70-1 3,4-dimethoxyphenylglyoxylic acid 
• 191998-16-0 Amino-(3,4-dimethoxy-phenyl)-acetic acid methyl ester 
• 850794-56-8 methyl 2-(3,4-dimethoxyphenyl)-2,3-epoxypropanoate 

Relevant articles and documents

Catalytic Activation of Carbon-Hydrogen Bonds in Lignin Linkages over Strong-Base-Modified Covalent Triazine Frameworks for Lignin Oxidative Cleavage

The design of highly efficient catalysts for the cleavage of various lignin linkages is the key step in the depolymerization of lignin. In this paper, strong-base-modified covalent triazine frameworks (CTFs) were reported to be effective in the cleavage o

New method for preparing alpha-bromo-3,4-dimethoxyphenylacetic trichloroethanol ester

The invention discloses a method for preparing a key intermediate alpha-bromo-3,4-dimethoxyphenylacetic trichloroethanol ester for synthesis of Baculiferin L. the method comprises the following steps:1) using 1,2-dimethoxylphenyl (CAS: 91-16-7) and methyl

Development of a simple system for the oxidation of electron-rich diazo compounds to ketones

Mild heating of diazo compounds in DMSO furnishes ketone products in moderate to excellent yields. The reaction is particularly effective on electron-rich substrates and exhibits high chemoselectivity, allowing for the use of diazo compounds containing additional oxidation-prone functional groups. This straightforward protocol offers an alternate route to synthetically useful α-ketoesters from readily available aryl diazoacetates.