| Identification | More | [Name]
1-(2-AMINOPHENYL)PYRROLE | [CAS]
6025-60-1 | [Synonyms]
1-(2-AMINOPHENYL)-1H-PYRROLE
1-(2-AMINOPHENYL)PYRROLE
2-(1H-PYRROL-1-YL)ANILINE
Benzenamine, 2-(1H-pyrrol-1-yl)-
N-(2-Aminophenyl)pyrrole
2-(1-Pyrrolyl)aniline
1-(2-AMINOPHENYL)PYRROLE, 98+%
1-(o-Aminophenyl)-1H-pyrrole
2-(1H-Pyrrol-1-yl)benzenamine | [EINECS(EC#)]
227-884-2 | [Molecular Formula]
C10H10N2 | [MDL Number]
MFCD00005344 | [Molecular Weight]
158.2 | [MOL File]
6025-60-1.mol |
| Chemical Properties | Back Directory | [Appearance]
LIGHT BEIGE TO BROWN CRYSTAL. POWDER AND NEEDLES | [Melting point ]
96-98 °C(lit.) | [Boiling point ]
273.29°C (rough estimate) | [density ]
1.1192 (rough estimate) | [refractive index ]
1.6392 (estimate) | [storage temp. ]
Keep in dark place,Sealed in dry,Room Temperature | [form ]
solid | [pka]
2.09±0.10(Predicted) | [Water Solubility ]
Insoluble in water. | [BRN ]
1307631 | [CAS DataBase Reference]
6025-60-1(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
Xn | [Risk Statements ]
R20/21/22:Harmful by inhalation, in contact with skin and if swallowed .
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing . | [WGK Germany ]
3
| [PackingGroup ]
III | [HS Code ]
29339980 |
| Hazard Information | Back Directory | [Chemical Properties]
LIGHT BEIGE TO BROWN CRYSTAL. POWDER AND NEEDLES | [Uses]
1-(2-Aminophenyl)pyrrole was used in the synthesis of 4-substituted pyrrolo[1,2-a]quinoxaline derivatives. | [Uses]
1-(2-Aminophenyl)pyrrole is used in the synthesis of 4-substituted pyrrolo[1,2-a]quinoxaline derivatives. It participates in Pt(IV)-catalyzed hydroamination triggered cyclization reaction to yield fused pyrrolo [1,2-a] quinoxalines. It is also used as primary and secondary intermediates. They act as antileishmanial agents. | [General Description]
1-(2-Aminophenyl)pyrrole participates in Pt(IV)-catalyzed hydroamination triggered cyclization reaction to yield fused pyrrolo [1,2-a] quinoxalines. It reacts with aromatic or heteroaromatic aldehydes in ethanol and catalytic amounts of acetic acid to yield 4,5-dihydropyrrolo[1,2-a]quinoxalines. Thin films of poly(1-(2-aminophenyl)pyrrole) has been prepared via oxidative electropolymerization. |
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