Basic information Safety Supplier Related

1-(4-NITROPHENYL)-1H-PYRROLE

Basic information Safety Supplier Related

1-(4-NITROPHENYL)-1H-PYRROLE Basic information

Product Name:
1-(4-NITROPHENYL)-1H-PYRROLE
Synonyms:
  • 1-(4-NITROPHENYL)-1H-PYRROLE
  • 1-(4-NITROPHENYL)PYRROLE
  • Nitrophenyl-(1H)-pyrrole
  • 1-(4-NITROPHENYL)-1H-PYRROLE 95%
  • N-hydroxy-4-(1-pyrrolyl)benzeneamine oxide
  • N-hydroxy-4-pyrrol-1-ylbenzeneamine oxide
  • N-hydroxy-4-pyrrol-1-yl-benzeneamine oxide
  • N-oxido-N-(4-pyrrol-1-ylphenyl)hydroxylamine
CAS:
4533-42-0
MF:
C10H8N2O2
MW:
188.18
Product Categories:
  • Building Blocks
  • Heterocyclic Building Blocks
  • Pyrroles
  • Functional Materials
  • Pyrroles (for Conduting Polymer Research)
  • Reagents for Conducting Polymer Research
  • pyrrole
Mol File:
4533-42-0.mol
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1-(4-NITROPHENYL)-1H-PYRROLE Chemical Properties

Melting point:
180-183 °C(lit.)
storage temp. 
Store at Room Tem.
form 
powder to crystal
color 
Light yellow to Yellow to Orange
CAS DataBase Reference
4533-42-0(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
2933998090

MSDS

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1-(4-NITROPHENYL)-1H-PYRROLE Usage And Synthesis

Synthesis

696-59-3

100-01-6

4533-42-0

General procedure: 4-nitroaniline (1 mmol), 2,5-dimethoxytetrahydrofuran (1.1 mmol) and L-(+)-tartaric acid-choline chloride low eutectic solvent (DES, 1.5 g) were added to a 50 mL round-bottomed flask and the reaction mixture was stirred at 90°C. The reaction was carried out by thin-layer chromatography (TLC). The reaction process was monitored by thin layer chromatography (TLC). After completion of the reaction, the mixture was cooled to room temperature and the target product 1-(4-nitrophenyl)-1H-pyrrole was extracted with ethyl acetate. After evaporation of the solvent, the residue was purified by silica gel column chromatography to give the pure product. The low eutectic solvent (DES) was dried under vacuum and reused for the next cycle.

References

[1] Journal of the Iranian Chemical Society, 2011, vol. 8, # 3, p. 851 - 856
[2] Synlett, 2009, # 14, p. 2245 - 2248
[3] ChemCatChem, 2013, vol. 5, # 12, p. 3743 - 3749
[4] Journal of Molecular Liquids, 2014, vol. 198, p. 259 - 262,4
[5] Asian Journal of Chemistry, 2013, vol. 25, # 1, p. 501 - 504

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