Basic information Safety Supplier Related

4-(1H-PYRROL-1-YL)ANILINE

Basic information Safety Supplier Related

4-(1H-PYRROL-1-YL)ANILINE Basic information

Product Name:
4-(1H-PYRROL-1-YL)ANILINE
Synonyms:
  • 4-(1H-PYRROL-1-YL)ANILINE
  • 1-(4-AMINOPHENYL)PYRROLE
  • ASISCHEM A93505
  • BUTTPARK 98\12-84
  • 4-(1-Pyrrolyl)aniline
  • 4-Pyrrol-1-yl-aniline
  • 4-Pyrrol-1-yl-phenylamine
  • Benzenamine, 4-(1H-pyrrol-1-yl)-
CAS:
52768-17-9
MF:
C10H10N2
MW:
158.2
Mol File:
52768-17-9.mol
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4-(1H-PYRROL-1-YL)ANILINE Chemical Properties

Melting point:
81 °C
Boiling point:
307.8±25.0 °C(Predicted)
Density 
1.09±0.1 g/cm3(Predicted)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
pka
3.36±0.10(Predicted)
Appearance
Off-white to light yellow Solid
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36/37/39
HazardClass 
IRRITANT
HS Code 
2933998090
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4-(1H-PYRROL-1-YL)ANILINE Usage And Synthesis

Synthesis

4533-42-0

52768-17-9

Under standard reaction conditions, 5.0 mg of Pd-gCN catalyst (containing 5.0 wt% Pd) was added to an ethanol solution (2 mL) containing 1.0 mM 1-(4-nitrophenyl)-1H-pyrrole, followed by the addition of 2 mM (1.2 eq., 0.07 mL) of 60% hydrazine hydrate solution. The reaction mixture was transferred to a 10 mL round bottom flask and reacted at reflux temperature (70 °C) for 4 hours. After completion of the reaction, the mixture was cooled to room temperature and the catalyst was isolated by filtration. The filtrate was purified by silica gel column chromatography to give 4-(1-pyrrolyl)aniline. For dinitroaromatic substrates, 4.0 mM (2.4 eq., 0.14 mL) of 60% hydrazine hydrate solution is required.

References

[1] Applied Catalysis A: General, 2016, vol. 523, p. 31 - 38
[2] European Journal of Medicinal Chemistry, 2015, vol. 96, p. 369 - 380
[3] Zeitschrift fur Naturforschung - Section B Journal of Chemical Sciences, 1996, vol. 51, # 6, p. 757 - 764
[4] Recueil des Travaux Chimiques des Pays-Bas, 1943, vol. 62, p. 177,181, 183
[5] Farmaco, Edizione Scientifica, 1983, vol. 38, # 4, p. 219 - 231

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