ChemicalBook--->CAS DataBase List--->52768-17-9

52768-17-9

52768-17-9 Structure

52768-17-9 Structure
IdentificationBack Directory
[Name]

4-(1H-PYRROL-1-YL)ANILINE
[CAS]

52768-17-9
[Synonyms]

ASISCHEM A93505
BUTTPARK 98\12-84
4-(1-Pyrrolyl)aniline
4-Pyrrol-1-yl-aniline
1-(4-AMINOPHENYL)PYRROLE
4-(1H-PYRROL-1-YL)ANILINE
4-Pyrrol-1-yl-phenylamine
Benzenamine, 4-(1H-pyrrol-1-yl)-
[Molecular Formula]

C10H10N2
[MDL Number]

MFCD01934575
[MOL File]

52768-17-9.mol
[Molecular Weight]

158.2
Chemical PropertiesBack Directory
[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
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H332-H335
[Precautionary statements ]

P261-P280-P305+P351+P338
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26-36/37/39
[Hazard Note ]

Irritant
[HazardClass ]

IRRITANT
[HS Code ]

2933998090
Spectrum DetailBack Directory
[Spectrum Detail]

4-(1H-PYRROL-1-YL)ANILINE(52768-17-9)1HNMR
Hazard InformationBack Directory
[Synthesis]

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

4533-42-0

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

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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