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53662-83-2

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53662-83-2 Usage

Description

2,5-Furandicarboxylic acid diethyl ester, with the CAS number 53662-83-2, is a white solid compound that is valuable in the field of organic synthesis. It is derived from furan, a heterocyclic compound with a wide range of applications in various industries due to its unique chemical properties.

Uses

Used in Organic Synthesis:
2,5-Furandicarboxylic acid diethyl ester is used as an intermediate in the synthesis of various organic compounds. Its unique structure allows for the creation of a diverse range of products, making it a versatile building block in the chemical industry.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,5-Furandicarboxylic acid diethyl ester is used as a key component in the development of new drugs. Its chemical properties enable the formation of novel drug candidates with potential therapeutic applications.
Used in Polymer Industry:
2,5-Furandicarboxylic acid diethyl ester is also utilized in the polymer industry for the production of bio-based and biodegradable polymers. These polymers have a lower environmental impact compared to traditional petroleum-based plastics, making them an attractive option for sustainable materials development.
Used in Chemical Research:
In the field of chemical research, 2,5-Furandicarboxylic acid diethyl ester serves as a model compound for studying various reaction mechanisms and exploring new synthetic routes. Its unique properties make it an ideal candidate for understanding the behavior of furan-based compounds under different reaction conditions.
Overall, 2,5-Furandicarboxylic acid diethyl ester is a versatile compound with a wide range of applications across various industries, including organic synthesis, pharmaceuticals, polymers, and chemical research. Its unique chemical properties and potential for sustainable development make it an important compound for future innovations.

Check Digit Verification of cas no

The CAS Registry Mumber 53662-83-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,6,6 and 2 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 53662-83:
(7*5)+(6*3)+(5*6)+(4*6)+(3*2)+(2*8)+(1*3)=132
132 % 10 = 2
So 53662-83-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H12O5/c1-3-13-9(11)7-5-6-8(15-7)10(12)14-4-2/h5-6H,3-4H2,1-2H3

53662-83-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name diethyl furan-2,5-dicarboxylate

1.2 Other means of identification

Product number -
Other names Diethyl 2,5-furandicarboxylate

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:53662-83-2 SDS

53662-83-2Relevant articles and documents

Method for preparation of 2, 5-furandicarboxylic acid diester compound from 5-hydroxymethylfurfural

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Paragraph 0025-0026; 0034-0035, (2019/12/31)

The invention discloses a method for preparation of a 2, 5-furandicarboxylic acid diester compound from 5-hydroxymethylfurfural. The method uses a cheap and specific non-noble metal as the catalyst, and adopts cheap and easily available oxygen or air as an oxygen source to prepare high purity dimethyl furan-2, 5-dicarboxylate at high efficiency under mild reaction conditions, thus solving the problems of low reaction efficiency, low product yield, high cost and the like in the prior art, and has good application prospects.

METHODS FOR PREPARING 2,5-FURANDICARBOXYLIC ACID

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Paragraph 0265; 0266: 0267; 0268, (2013/04/13)

Provided are methods of producing 2,5-furandicarboxylic acid (FDCA) from renewable sources such as seaweed, alginate, oligoalginate, pectin, oligopectin, polygalacturonate, galacturonate, and/or oligogalacturonate. The sugars in the renewable sources can be converted into one or more intermediates such as 4-deoxy-L-erythro-5- hexoseulose uronate (DEHU), 4-deoxy-L-threo-5-hexosulose uronate (DTHU), 5- hydroxymethyl furfural (HMF), 2,5-dihydroxymethyl furan (DHMF), and 5-formyl-2- furancarboxylic acid (FFA), which can be converted into FDCA by dehydration and cyclization to produce 5-formyl-2-furancarboxylic acid (FFA), followed by oxidation to produce FDCA. DEHU or DTHU may also be converted into FDCA by oxidation to produce 2,3-dihydroxy-5-oxohexanedioic acid (DOHA), which then undergoes dehydration and cyclization to produce FDCA.

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