1-(2-Aminophenyl)pyrrole, 98+%
1-(2-Aminophenyl)pyrrole, 98+%
1-(2-Aminophenyl)pyrrole, 98+%
Thermo Scientific Chemicals

1-(2-Aminophenyl)pyrrole, 98+%

CAS: 6025-60-1 | C10H10N2 | 158.204 g/mol
Have Questions?
Change viewbuttonViewtableView
Quantity:
1 g
5 g
Catalog number L06887.03
also known as L06887-03
Price (USD)
34.50
Each
Quantity:
1 g
Request bulk or custom format
Price (USD)
34.50
Each
Chemical Identifiers
CAS6025-60-1
IUPAC Name2-(1H-pyrrol-1-yl)aniline
Molecular FormulaC10H10N2
InChI KeyGDMZHPUPLWQIBD-UHFFFAOYSA-N
SMILESNC1=CC=CC=C1N1C=CC=C1
View more
SpecificationsSpecification SheetSpecification Sheet
Identification (FTIR)Conforms
Appearance (Color)White to cream to pale brown or pale yellow
Assay (GC)≥98.0%
Melting Point (clear melt)93.5-99.5?C
FormCrystals or powder or crystalline powder
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.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
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.

Solubility
Insoluble in water.

Notes
Incompatible materials are oxidizing agents, acids, Acid chlorides, Acid anhydrides, Chloroformates. Store in cool place. Keep container tightly closed in a dry and well-ventilated place.
RUO – Research Use Only
Kasem K. Kasem; Sara Menges; Stephenie Jones. Photoelectrochemical studies on poly[1-(2-aminophenyl)pyrrole] — Creation of a photoactive inorganic-organic semiconductor interface (IOI).Canadian Journal of Chemistry.2005,87 (8), 1109-1116..