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5-(Ethoxycarbonyl)furan-2-carboxylic acid is a chemical compound with the molecular formula C8H8O5. It is a derivative of furan-2-carboxylic acid, featuring an ethoxycarbonyl group attached to the 5-position of the furan ring. This organic compound is characterized by its five-membered furan ring, which contains one oxygen atom, and a carboxylic acid group at the 2-position. The ethoxycarbonyl group, an ester functional group, is attached to the 5-position, providing additional functionality to the molecule. 5-(ethoxycarbonyl)furan-2-carboxylic acid is of interest in organic synthesis and may have potential applications in the development of pharmaceuticals or other chemical products due to its unique structure and reactivity.

32933-01-0

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32933-01-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 32933-01-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,9,3 and 3 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 32933-01:
(7*3)+(6*2)+(5*9)+(4*3)+(3*3)+(2*0)+(1*1)=100
100 % 10 = 0
So 32933-01-0 is a valid CAS Registry Number.

32933-01-0SDS

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 5-(Ethoxycarbonyl)-2-furoic acid

1.2 Other means of identification

Product number -
Other names furan-2,5-dicarboxylic acid diamide

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:32933-01-0 SDS

32933-01-0Relevant academic research and scientific papers

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.

METHOD FOR THE PREPARATION OF 2,5-FURANDICARBOXYLIC ACID AND ESTERS THEREOF

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Page/Page column 6; 7; 11, (2011/04/26)

The application describes a method for the preparation of 2,5-furandicarboxylic acid ("FDCA") and/or an alkyl ester of FDCA comprising the step of contacting a feed comprising a starting material selected from 5-alkoxymethylfurfural, 2,5-di(alkoxymethyl)furan and a mixture thereof with an oxidant in the presence of an oxidation catalyst. The feed may also comprise 5-hydroxymethylfurfural as a further starting material.

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