70175-90-5

Basic information

• Product Name: 2-[4-(4-METHOXY-PHENOXY)-PHENYL]-MALONIC ACID MONO-(4-METHOXY-PHENYL) ESTER
• Synonyms: 2-[4-(4-METHOXY-PHENOXY)-PHENYL]-MALONIC ACID MONO-(4-METHOXY-PHENYL) ESTER;[4-[(4-Methoxyphenyl)methoxy]phenyl]propanedioic acid mono[(4-methoxyphenyl)methyl] ester;2-[4-[(4-Methoxyphenyl)methoxy]phenyl]propanedioic acid 1-[(4-methoxyphenyl)methyl] ester;3-(4-Methoxyphenoxy)-2-(4-(4-Methoxyphenoxy)phenyl)-3-oxopropanoic acid;2-[4-[(4-Methoxyphenyl)Methoxy]phenyl]propanedio;2-(4-Methoxybenzyl)-2-[4-(4-Methoxybenzyloxy)phenyl]acetic acid;2-[4-[(4-Methoxyphenyl)methoxy]phenyl]propanedioic acid 1-[(4-methoxyphenyl)methyl] ester [4-[(4-Methoxyphenyl)methoxy]phenyl]propanedioic acid mono[(4-methoxyphenyl)methyl] ester
• CAS NO: 70175-90-5
• Molecular Formula: C₂₅H₂₄O₇
• Molecular Weight: 408.41
• EINECS: 1533716-785-6
• Mol File: 70175-90-5.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• Density: 1.255
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 2-[4-(4-METHOXY-PHENOXY)-PHENYL]-MALONIC ACID MONO-(4-METHOXY-PHENYL) ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[4-(4-METHOXY-PHENOXY)-PHENYL]-MALONIC ACID MONO-(4-METHOXY-PHENYL) ESTER(70175-90-5)
• EPA Substance Registry System: 2-[4-(4-METHOXY-PHENOXY)-PHENYL]-MALONIC ACID MONO-(4-METHOXY-PHENYL) ESTER(70175-90-5)

Safety Data

• Hazardous Substances Data: 70175-90-5(Hazardous Substances Data)

Usage

General Description

2-[4-(4-Methoxy-phenoxy)-phenyl]-malonic acid mono-(4-methoxy-phenyl) ester is a chemical compound categorized under the class of organic compounds known as diphenyl ethers. These are aromatic compounds containing two phenyl groups separated by an ether group. The 4-methoxy-phenoxy and 4-methoxy-phenyl functional groups indicate the presence of a methoxy group (-OCH3) attached to a phenol or phenyl ring. As a malonic acid mono-ester, it contains malonic acid, which is a dicarboxylic acid, partially esterified. The exact properties of this compound, such as its physical characteristics, reactivity, and uses, are not provided, and would require further specific scientific research.

Upstream product

• 105-13-5 4-Methoxybenzyl alcohol 
• 156-38-7 4-hydroxyphenylacetate 
• 124-38-9 carbon dioxide 

Downstream Products

• 75007-71-5 C₂₀H₂₀N₆O₉S 
• 73973-65-6 (6R,7R)-7-Methoxy-7-{2-(4-methoxy-benzyloxycarbonyl)-2-[4-(4-methoxy-benzyloxy)-phenyl]-acetylamino}-3-(1-methyl-1H-tetrazol-5-ylsulfanylmethyl)-8-oxo-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid benzyl ester 

Relevant articles and documents

Method for synthesizing latamoxef side chain

The invention relates to a method for synthesizing a latamoxef side chain. The method comprises the following steps: 1. dissolving p-hydroxyphenylacetic acid and p-methoxybenzyl alcohol in an inert solvent and using immobilized lipase to perform biocatalytic esterification in a reactor, and obtain a latamoxef side chain intermediate I after dewatering; 2. dissolving the latamoxef side chain intermediate I and p-methoxybenzyl alcohol in an inert solvent and using immobilized laccase to perform biocatalytic etherification to obtain a latamoxef side chain intermediate II; 3. subjecting the latamoxef side chain intermediate II to carbonylation to obtain the latamoxef side chain 4-(4-methoxybenzyloxy)phenylmalonic acid-4-methoxybenzyl monoester. The synthesis method solves the environmental protection problem of generating large amount of waste acid water and alkaline waste residues, and has the advantages of simultaneously reducing the energy consumption and the production cost, and increasing the yield and purity of the product.