Furantetracarboxylic acid

Base Information

• Chemical Name: Furantetracarboxylic acid
• CAS No.: 20416-04-0
• Molecular Formula: C8H4 O9
• Molecular Weight: 244.114
• NSC Number: 41309
• UNII: 526V46EZC7
• DSSTox Substance ID: DTXSID40285293
• Nikkaji Number: J103.135J
• Wikipedia: Furantetracarboxylic_acid
• Wikidata: Q5509477
• Pharos Ligand ID: NS4MC1PA2S2T
• ChEMBL ID: CHEMBL1742368
• Mol file: 20416-04-0.mol

Synonyms:Furantetracarboxylic acid;20416-04-0;2,3,4,5-Furantetracarboxylic acid;furan-2,3,4,5-tetracarboxylic acid;NSC-41309;NSC41309;526V46EZC7;NCIStruc1_000427;NCIStruc2_000574;UNII-526V46EZC7;SCHEMBL1582401;CHEMBL1742368;2,4,5-Furantetracarboxylic acid;DTXSID40285293;NCI41309;CCG-37882;NCGC00013480;NCGC00013480-02;NCGC00096595-01;NCI60_003936;AE-562/43458255;Q5509477

Chemical Property of Furantetracarboxylic acid

Chemical Property:

• Vapor Pressure: 1.61E-15mmHg at 25°C
• Boiling Point: 605.6°Cat760mmHg
• Flash Point: 320.1°C
• PSA: 162.34000
• Density: 1.995g/cm³
• LogP: 0.07240
• XLogP3: -0.2
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 9
• Rotatable Bond Count: 4
• Exact Mass: 243.98553170
• Heavy Atom Count: 17
• Complexity: 351

Purity/Quality:

99.0%min ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1(=C(OC(=C1C(=O)O)C(=O)O)C(=O)O)C(=O)O

Technology Process of Furantetracarboxylic acid

There total 2 articles about Furantetracarboxylic acid which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

tetraethyl furan-2,3,4,5-tetracarboxylate (20416-03-9) → furantetracarboxylic acid (20416-04-0)

Guidance literature:

With hydrogenchloride; acetic acid;

DOI:10.1002/hlca.19330160138

Reference yield:

→ furantetracarboxylic acid (20416-04-0)

Guidance literature:

Aus Tetracarboxylat I;

Reference yield:

furantetracarboxylic acid (20416-04-0) → 2,4-furan dicarboxylic acid (4282-28-4)

Guidance literature:

Multi-step reaction with 3 steps

1: copper-powder; quinoline

2: boron fluoride ether adduct

3: aq. NaOH solution; potassium permanganate

With quinoline; sodium hydroxide; potassium permanganate; boron fluoride ether; copper;

DOI:10.1002/hlca.19570400404

upstream raw materials:

tetraethyl furan-2,3,4,5-tetracarboxylate

Downstream raw materials:

3-Furoic acid

furan-3,4-dicarboxylic acid

furan-2,3,4-tricarboxylic acid

methyl furan-3-carboxylate