All Photos(1)
Synonym(s):
5-Nitrofurfural
Empirical Formula (Hill Notation):
C5H3NO4
CAS Number:
Molecular Weight:
141.08
Beilstein:
120539
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
99%
form
solid
refractive index
n20/D 1.59 (lit.)
bp
121 °C/10 mmHg (lit.)
mp
37-39 °C (lit.)
density
1.349 g/mL at 25 °C (lit.)
SMILES string
[H]C(=O)c1ccc(o1)[N+]([O-])=O
InChI
1S/C5H3NO4/c7-3-4-1-2-5(10-4)6(8)9/h1-3H
InChI key
SXINBFXPADXIEY-UHFFFAOYSA-N
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Related Categories
Application
5-Nitro-2-furaldehyde was used in the synthesis of a series of 4-(5-nitrofuran-2-yl)prop-2-en-1-one derivatives. It was also used in the synthesis of modified mesoporous silica (MCM-41).
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Flam. Sol. 1
WGK
WGK 3
Flash Point(F)
91.4 °F
Flash Point(C)
33 °C
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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H Cerecetto et al.
European journal of medicinal chemistry, 35(3), 343-350 (2000-04-29)
Several novel semicarbazone derivatives were prepared from 5-nitro-2-furaldehyde or 5-nitrothiophene-2-carboxaldehyde and semicarbazides bearing a spermidine-mimetic moiety. All derivatives presented the E-configuration, as determined by NMR-NOE experiments. These compounds were tested in vitro as potential antitrypanosomal agents, and some of them
Jarosław Lewkowski et al.
Chemosphere, 188, 618-632 (2017-09-17)
Since aminophosphonate-based herbicides like glyphosate are currently one of the most popular and widely applied active agent in agrochemistry, there is an urgent need for searching new compounds among this family with potential herbicidal activity, but exhibiting low toxicity against
Broad specificity indirect competitive immunoassay for determination of nitrofurans in animal feeds.
Jun Li et al.
Analytica chimica acta, 678(1), 1-6 (2010-09-28)
A generic hapten of nitrofurans was synthesized by derivatization of 5-nitrofurfural with diamine, and the hapten was coupled to carrier protein to prepare different immunogens and coating antigens by using diazotization method and glutaraldehyde method. The obtained novel polyclonal antibodies
A Cisak et al.
Acta poloniae pharmaceutica, 58(6), 427-434 (2002-08-29)
5-Nitro-2-furaldehyde (NFA) forms in alkaline solutions an anion of nitronic acid of (5-nitro-furan-2-yl)-methanediol. Upon acidification (5-nitro-furan-2-yl)-methanediol (HNFA) appears with pKa=4.6. Then, in a novel irreversible redox ring-opening reaction, nitrile oxide of alpha-ketoglutaconic acid is formed which hydrolyses in acidic solutions.
M I Walash et al.
Acta pharmaceutica Hungarica, 64(1), 5-8 (1994-01-01)
A first derivative (1D) spectrophotometric method is described for the determination of furazolidone in the presence of its degradation product (5-nitrofuraldehyde). The method was based on the direct measurement at the maximum of the first derivative curve for furazolidone at
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