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5-(4-Nitrophenyl)-2-furaldehyde

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5-(4-Nitrophenyl)-2-furaldehyde Basic information

Product Name:
5-(4-Nitrophenyl)-2-furaldehyde
Synonyms:
  • 5-(4-NITROPHENYL)-2-FURANCARBOXALDEHYDE
  • 5-(4-NITROPHENYL)-2-FURALDEHYDE
  • 5-(4-NITRO-PHENYL)-FURAN-2-CARBALDEHYDE
  • 5-(4-NITROPHENYL)-FURAN-2-CARBOXALDHYDE
  • 5-(4-NITROPHENYL)FURFURAL
  • 5-(p-Nitropheny) Furancarboxaldehyde
  • Nitrophenyl-2-furancarboxaldehyde
  • 5-(4-Nitrophenyl)-2-Furancarbo
CAS:
7147-77-5
MF:
C11H7NO4
MW:
217.18
EINECS:
230-459-4
Product Categories:
  • Aromatic Aldehydes & Derivatives (substituted)
  • Amines
  • Aromatics
  • Heterocycles
  • Intermediates & Fine Chemicals
  • Pharmaceuticals
  • Building Blocks
  • C10-C12
  • C8 to C11
  • Carbonyl Compounds
  • Chemical Synthesis
  • Furans
  • Heterocyclic Building Blocks
  • Organic Building Blocks
  • Aldehydes
  • Furans, Benzofurans & Dihydrobenzofurans
  • Furans, Benzofurans & Dihydrobenzofurans
Mol File:
7147-77-5.mol
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5-(4-Nitrophenyl)-2-furaldehyde Chemical Properties

Melting point:
204-206 °C(lit.)
Boiling point:
406.8±35.0 °C(Predicted)
Density 
1.348±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
solubility 
DMSO (Slightly, Heated), Ethyl Acetate (Slightly, Heated)
form 
Solid
color 
Yellow to Dark Yellow
Major Application
pharmaceutical (small molecule)
InChI
InChI=1S/C11H7NO4/c13-7-10-5-6-11(16-10)8-1-3-9(4-2-8)12(14)15/h1-7H
InChIKey
RTSOJVJDKNKNFU-UHFFFAOYSA-N
SMILES
O1C(C2=CC=C([N+]([O-])=O)C=C2)=CC=C1C=O
CAS DataBase Reference
7147-77-5(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xn,Xi
Risk Statements 
22-36/37/38
Safety Statements 
26-36
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
29329990
Storage Class
11 - Combustible Solids

MSDS

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5-(4-Nitrophenyl)-2-furaldehyde Usage And Synthesis

Chemical Properties

brown crystalline powder

Uses

A furfural nitrophenyl derivative as antibacterial and fungistatic agent.

Synthesis

98-01-1

100-01-6

7147-77-5

The target compounds 5-(4-nitrophenyl)furan-2-carbaldehyde (1-9) were synthesized and structurally characterized using 2-furancarboxaldehyde and 4-nitroaniline as starting materials with reference to the methods described in literature [3,13].

References

[1] Heterocyclic Communications, 2003, vol. 9, # 6, p. 625 - 628
[2] Tetrahedron, 2013, vol. 69, # 48, p. 10292 - 10298
[3] Chinese Journal of Chemistry, 2014, vol. 32, # 7, p. 637 - 644
[4] New Journal of Chemistry, 2015, vol. 39, # 9, p. 7206 - 7210
[5] Asian Journal of Chemistry, 2013, vol. 25, # 14, p. 7738 - 7742

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