170968
5-Nitro-2-furaldehyde
99%
Synonym(s):
5-Nitrofurfural
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About This Item
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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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.)
functional group
aldehyde
nitro
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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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
Storage Class Code
4.1B - Flammable solid hazardous materials
WGK
WGK 3
Flash Point(F)
91.4 °F - closed cup
Flash Point(C)
33 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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
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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
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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
Seyed Reza Yousefi et al.
Talanta, 80(1), 212-217 (2009-09-29)
A new synthesized modified mesoporous silica (MCM-41) using 5-nitro-2-furaldehyde (fural) was applied as an effective sorbent for the solid phase extraction of uranium(VI) and thorium(IV) ions from aqueous solution for the measurement by inductively coupled plasma optical emission spectrometry (ICP
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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