Sigma Aldrich H40807 5-Hydroxymethyl-2-furaldehyde 99% 5 gr
Category
Brand
Stock Code
LB.SA.H40807-5G
Kısa Bilgi
Synonym(s): 2-Methoxyphenol, Catechol monomethyl ether, Pyrocatechol monomethyl ether Linear Formula: (CH3O)C6H4OH CAS Number: 90-05-1 Molecular Weight: 124.14 Beilstein: 508112 EC Number: 201-964-7 MDL number: MFCD00002185 PubChem Substance ID: 24895212 NACRES: NA.77
Market Price
CAS Number: 67-47-0
| Sigma Aldrich H40807 5-Hydroxymethyl-2-furaldehyde 99% 5 gr |
| Synonym(s): 5-(Hydroxymethyl)furfural, 5-Hydroxymethyl-2-furancarboxaldehyde, HMF Empirical Formula (Hill Notation): C6H6O3 CAS Number: 67-47-0 Molecular Weight: 126.11 Beilstein: 110889 EC Number: 200-654-9 MDL number: MFCD00003234 PubChem Substance ID: 24895618 NACRES: NA.22 |
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PROPERTIES
Quality Level 200
Assay 99% refractive index n20/D 1.562 (lit.) bp 114-116 °C/1 mmHg (lit.) mp 28-34 °C (lit.) density 1.243 g/mL at 25 °C (lit.) storage temp. 2-8°C SMILES string [H]C(=O)c1ccc(CO)o1 InChI 1S/C6H6O3/c7-3-5-1-2-6(4-8)9-5/h1-3,8H,4H2 InChI key NOEGNKMFWQHSLB-UHFFFAOYSA-N DESCRIPTION
Application
5-Hydroxymethyl-2-furaldehyde (HMF) can be used in the synthesis of: - Furan-2,5-dicarboxaldehyde (FDA) using a vanadyl phosphate-based catalyst via selective oxidation.[1] - Prepolymer and antiviral precursor, 5,5′-oxy(bismethylene)-2-furaldehyde (OBMF) using solid acid catalysts via etherification reaction.[2] - Diformylfurane (DFF) by aerobic oxidation using pyridine-vanadyl complexes.[3] |
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