728373
2,5-呋喃二甲醛
97%
别名:
2,5-二甲酰呋喃, 2,5-呋喃甲醛, 5-甲酰糠醛
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关于此项目
经验公式（希尔记法）:
C6H4O3
化学文摘社编号:
分子量:
124.09
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
212-520-7
Beilstein/REAXYS Number:
109424
MDL number:
产品名称
2,5-呋喃二甲醛, 97%
InChI key
PXJJKVNIMAZHCB-UHFFFAOYSA-N
InChI
1S/C6H4O3/c7-3-5-1-2-6(4-8)9-5/h1-4H
SMILES string
O=Cc1ccc(C=O)o1
assay
≥96.5% (HPLC)
97%
form
powder
functional group
aldehyde
storage temp.
−20°C
Quality Level
Application
2,5-呋喃二甲醛可作为结构单元，与壳聚糖发生界面聚合反应制备可持续薄膜复合材料（TFC）膜。
2,5-呋喃二甲醛可与壳聚糖发生界面聚合反应合成可持续薄–膜复合材料（TFC）膜，还可用作Hg2+离子的荧光化学传感器。
General description
2,5-呋喃二甲醛是5-羟甲基糠醛的氧化产物。它被用作化学合成中的有机结构单元。它也可作为生产有价值的生物聚合物的前体。
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Selective photocatalytic oxidation of 5-hydroxymethyl-2-furfural to 2, 5-furandicarboxyaldehyde in aqueous suspension of g-C3N4
Krivtsov, et al.
Applied Catalysis. B, Environmental, 204, 430-439 (2017)
Solvent-resistant thin-film composite membranes from biomass-derived building blocks: chitosan and 2, 5-furandicarboxaldehyde
Park, et al.
ACS sustainable chemistry & engineering, 10, 998-1007 (2021)
A bis-hydrazone derivative of 2, 5-furandicarboxaldehyde with perfect hetero-atomic cavity for selective sensing of Hg (II) and its intracellular detection in living HeLa S3 cell
Kumari, et al.
Sensors and Actuators B, Chemical, 243, 1181-1190 (2017)
Alessandro Allegri et al.
Molecules (Basel, Switzerland), 25(22) (2020-11-14)
The photocatalytic oxidation of biomass-derived building blocks such as 5-hydroxymethylfurfural (HMF) is a promising reaction for obtaining valuable chemicals and the efficient long-term storage of solar radiation. In this work, we developed innovative TiO2-based materials capable of base-free HMF photo-oxidation
Maria Ventura et al.
ChemSusChem, 11(8), 1305-1315 (2018-03-08)
Mixed oxides based on MgO⋅CeO2 were used as efficient catalysts in the aerobic oxidation of 5-hydroxymethylfurfural (5-HMF) to afford, with very high selectivity, either 2,5-diformylfuran (DFF, 99 %) or 2-formyl-5-furancarboxylic acid (FFCA, 90 %), depending on the reaction conditions. 5-Hydroxymethyl-2-furancarboxylic acid (HMFCA
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