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1710-13-0

3,5-Furandicarboxylic acid dimethyl ester, also known as FDCA-dimethyl ester, is a chemical compound derived from 3,5-furandicarboxylic acid (FDCA), a key building block for the production of polyethylene furanoate (PEF), a bio-based and biodegradable alternative to petroleum-based polyethylene terephthalate (PET). FDCA-dimethyl ester is formed by the esterification of FDCA with methanol, resulting in a colorless liquid with a molecular formula of C8H10O5. 3,5-Furandicarboxylic acid dimethyl ester is of significant interest in the field of sustainable chemistry due to its potential use in the development of eco-friendly materials and its role in reducing reliance on fossil fuels.

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  • 1710-13-0 Structure

  • Basic information

    1. Product Name: 3,5-Furandicarboxylic acid dimethyl ester
    2. Synonyms: 2,4-Furandicarboxylic acid dimethyl ester;3,5-Furandicarboxylic acid dimethyl ester;Furan-2,4-dicarboxylic acid dimethyl ester
    3. CAS NO:1710-13-0
    4. Molecular Formula: C8H8O5
    5. Molecular Weight: 184.15
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1710-13-0.mol

  • Chemical Properties

    1. Melting Point: 104-107 °C
    2. Boiling Point: 265.3±20.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.244±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3,5-Furandicarboxylic acid dimethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,5-Furandicarboxylic acid dimethyl ester(1710-13-0)
    11. EPA Substance Registry System: 3,5-Furandicarboxylic acid dimethyl ester(1710-13-0)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1710-13-0(Hazardous Substances Data)

1710-13-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1710-13-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,1 and 0 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1710-13:
(6*1)+(5*7)+(4*1)+(3*0)+(2*1)+(1*3)=50
50 % 10 = 0
So 1710-13-0 is a valid CAS Registry Number.

1710-13-0Relevant articles and documents

Concurrent formation of furan-2,5- and furan-2,4-dicarboxylic acid: Unexpected aspects of the Henkel reaction

Thiyagarajan, Shanmugam,Pukin, Aliaksei,Van Haveren, Jacco,Lutz, Martin,Van Es, Daan S.

, p. 15678 - 15686 (2013/09/12)

The concurrent formation of furan-2,5- and furan-2,4-dicarboxylic acid under solvent free conditions via a disproportionation reaction is described. By reacting potassium-2-furoate at 260 °C in the presence of 22 mol% of (Lewis acidic) catalysts like CdI2 or ZnCl2, potassium-2-furoate is disproportionated to furan and furandicarboxylic acids. Besides furan and furan-2,5-dicarboxylic acid (2,5-FDCA) as the main products, furan-2,4-dicarboxylic acid (2,4-FDCA) is also formed as a by-product. Experimental evidence has been obtained that, under the reaction conditions applied, 2,5-FDCA and 2,4-FDCA are formed by separate reaction pathways. Selectivity towards the different FDCA isomers is affected by the type of catalyst used. Single-crystal X-ray analysis shows that 2,4-FDCA has a more 'linear' character compared to 2,5-FDCA and hence is structurally more comparable to terephthalic acid (TA), making it an interesting monomer for synthetic polyesters.

The scent of bacteria: Headspace analysis for the discovery of natural products

Citron, Christian A.,Rabe, Patrick,Dickschat, Jeroen S.

, p. 1765 - 1776 (2013/01/15)

Volatile compounds released by 50 bacterial strains, 45 of them actinobacteria in addition to three chloroflexi and two myxobacteria, have been collected by use of a closed-loop stripping apparatus, and the obtained headspace extracts have been analyzed by GC-MS. Excluding terpenes that have recently been published elsewhere, 254 compounds from all kinds of compound classes have been identified. For unambiguous compound identification several reference compounds have been synthesized. Among the detected volatiles 12 new natural products have been found, in addition to mellein, which was released by Saccharopolyspora erythraea. The iterative PKS for this compound has recently been identified by in vitro experiments, but mellein production in S. erythraea has never been reported before. These examples demonstrate that headspace analysis is an important tool for the discovery of natural products that may be overlooked using conventional techniques. The method is also useful for feeding experiments with isotopically labeled precursors and was applied to investigate the biosynthesis of the unusual nitrogen compound 1-nitro-2-methylpropane, which arises from valine. Furthermore, several streptomycetes emitted compounds that were previously recognized as insect pheromones, thus questioning if bacterial symbionts are involved in insect communication.

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