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
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
211-816-3
Beilstein/REAXYS Number:
120539
MDL number:
Assay:
99%
Form:
solid
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.)
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
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).
signalword
Danger
hcodes
Hazard Classifications
Flam. Sol. 1
Storage Class
4.1B - Flammable solid hazardous materials
wgk
WGK 3
flash_point_f
91.4 °F - closed cup
flash_point_c
33 °C - closed cup
ppe
Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
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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
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