728373
2,5-Furandicarboxaldehyde
97%
Synonyme(s) :
2,5-Diformylfuran, 2,5-Furandicarbaldehyde, 5-Formylfurfural
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About This Item
Formule empirique (notation de Hill) :
C6H4O3
Numéro CAS:
Poids moléculaire :
124.09
Beilstein:
109424
Numéro CE :
Numéro MDL:
Code UNSPSC :
12352100
ID de substance PubChem :
Nomenclature NACRES :
NA.22
Produits recommandés
Essai
≥96.5% (HPLC)
97%
Forme
powder
Groupe fonctionnel
aldehyde
Température de stockage
−20°C
Chaîne SMILES
O=Cc1ccc(C=O)o1
InChI
1S/C6H4O3/c7-3-5-1-2-6(4-8)9-5/h1-4H
Clé InChI
PXJJKVNIMAZHCB-UHFFFAOYSA-N
Description générale
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.
Mention d'avertissement
Warning
Mentions de danger
Conseils de prudence
Classification des risques
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Organes cibles
Respiratory system
Code de la classe de stockage
11 - Combustible Solids
Classe de danger pour l'eau (WGK)
WGK 3
Point d'éclair (°F)
Not applicable
Point d'éclair (°C)
Not applicable
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Selective photocatalytic oxidation of 5-hydroxymethyl-2-furfural to 2, 5-furandicarboxyaldehyde in aqueous suspension of g-C3N4
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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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