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CDS000126

Sigma-Aldrich

5-Formyl-2-furoic acid

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About This Item

Empirical Formula (Hill Notation):
C6H4O4
Molecular Weight:
140.09
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:

form

solid

SMILES string

OC(=O)c1ccc(C=O)o1

InChI

1S/C6H4O4/c7-3-4-1-2-5(10-4)6(8)9/h1-3H,(H,8,9)

InChI key

SHNRXUWGUKDPMA-UHFFFAOYSA-N

Other Notes

Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of unique chemicals. Sigma-Aldrich does not collect analytical data for this product. Buyer assumes responsibility to confirm product identity and/or purity. All sales are final.

NOTWITHSTANDING ANY CONTRARY PROVISION CONTAINED IN SIGMA-ALDRICH′S STANDARD TERMS AND CONDITIONS OF SALE OR AN AGREEMENT BETWEEN SIGMA-ALDRICH AND BUYER, SIGMA-ALDRICH SELLS THIS PRODUCT "AS-IS" AND MAKES NO REPRESENTATION OR WARRANTY WHATSOEVER WITH RESPECT TO THIS PRODUCT, INCLUDING ANY (A) WARRANTY OF MERCHANTABILITY; (B) WARRANTY OF FITNESS FOR A PARTICULAR PURPOSE; OR (C) WARRANTY AGAINST INFRINGEMENT OF INTELLECTUAL PROPERTY RIGHTS OF A THIRD PARTY; WHETHER ARISING BY LAW, COURSE OF DEALING, COURSE OF PERFORMANCE, USAGE OF TRADE OR OTHERWISE.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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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
Cristina Megías-Sayago et al.
Frontiers in chemistry, 8, 461-461 (2020-06-26)
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
Harrison B Rose et al.
International journal of pharmaceutics, 594, 120170-120170 (2020-12-15)
Determination of an equilibrium pH value in complex aqueous solution and deconvolution of this equilibrium to evaluate phenomena related to mixing, dilution, or progress of reaction is increasingly important in areas ranging from water quality to pharmaceutical formulations and manufacturing.
Zi-Wei Wang et al.
Bioresource technology, 303, 122930-122930 (2020-02-11)
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
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

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