728373
2,5-Furandicarboxaldehyde
97%
Synonym(s):
2,5-Diformylfuran, 2,5-Furandicarbaldehyde, 5-Formylfurfural
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About This Item
Empirical Formula (Hill Notation):
C6H4O3
CAS Number:
Molecular Weight:
124.09
Beilstein:
109424
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
≥96.5% (HPLC)
97%
form
powder
functional group
aldehyde
storage temp.
−20°C
SMILES string
O=Cc1ccc(C=O)o1
InChI
1S/C6H4O3/c7-3-5-1-2-6(4-8)9-5/h1-4H
InChI key
PXJJKVNIMAZHCB-UHFFFAOYSA-N
General description
2,5-Furandicarboxaldehyde is an oxidation product of 5-hydroxymethyl furfural. It is used as an organic building block in chemical synthesis. It is also used as a precursor for the production of valuable biopolymers.
Application
2,5- Furandicarboxaldehyde can be used in the synthesis of sustainable thin–film composite (TFC) membranes by interfacial polymerization reaction with chitosan and it also acts as a fluorescent chemo sensor for Hg2+ ions.
2,5-Furandicarboxaldehyde can be used as a building block in the fabrication of sustainable thin-film composite (TFC) membranes by the interfacial polymerization reaction with chitosan.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
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A series of gold catalysts supported on pure CeO2, ZrO2, and two different Ce-Zr mixed oxides have been prepared and tested in the 5-hydroxymethyl-2-furfural oxidation reaction. All catalysts show high catalytic activity (100% conversion) and important selectivity (27-41%) to the
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The main aim of this work was to firstly develop a selective oxidation approach for biologically converting 5-hydroxymethylfurfural and furfural into the corresponding furan-based carboxylic acids with recombinant Escherichia coli HMFOMUT. Whole-cells of this recombinant strain harbored good biocatalytic activity
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