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2-[4-(4-Methoxy-phenoxy)-phenyl]-malonic acid mono-(4-methoxy-phenyl) ester is a complex organic compound belonging to the diphenyl ether class. It features two phenyl groups connected by an ether linkage, with the presence of 4-methoxy-phenoxy and 4-methoxy-phenyl functional groups, indicating a methoxy group (-OCH3) attached to a phenol or phenyl ring. As a malonic acid mono-ester, it includes a partially esterified malonic acid, which is a dicarboxylic acid. Further scientific research is needed to determine its specific properties, reactivity, and potential applications.

70175-90-5

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70175-90-5 Usage

Uses

The provided materials do not specify the uses of 2-[4-(4-Methoxy-phenoxy)-phenyl]-malonic acid mono-(4-methoxy-phenyl) ester. However, given its classification as an organic compound and the presence of malonic acid and methoxy groups, it may have potential applications in various fields such as pharmaceuticals, materials science, or as an intermediate in chemical synthesis. Further research and experimentation would be required to confirm its practical applications and benefits.

Check Digit Verification of cas no

The CAS Registry Mumber 70175-90-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,1,7 and 5 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 70175-90:
(7*7)+(6*0)+(5*1)+(4*7)+(3*5)+(2*9)+(1*0)=115
115 % 10 = 5
So 70175-90-5 is a valid CAS Registry Number.

70175-90-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-Methoxyphenoxy)-2-(4-(4-methoxyphenoxy)phenyl)-3-oxopropanoic acid

1.2 Other means of identification

Product number -
Other names 3-(4-methoxyphenoxy)-2-[4-(4-methoxyphenoxy)phenyl]-3-oxopropanoic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:70175-90-5 SDS

70175-90-5Relevant academic research and scientific papers

Method for synthesizing latamoxef side chain

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Paragraph 0058; 0059; 0060; 0061, (2018/04/03)

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.

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