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1-(2-Aminophenyl)pyrrole, 98+%, Thermo Scientific Chemicals
Catalog number: L06887.03
1 g, Each
Thermo Scientific Chemicals
1-(2-Aminophenyl)pyrrole, 98+%, Thermo Scientific Chemicals
Catalog number: L06887.03
1 g, Each
Quantity
Catalog number: L06887.03
also known as L06887-03
Price (USD)
Price: 32.90
Online price: 27.65
Your price:
Quantity
-
Chemical Identifiers
CAS
6025-60-1
IUPAC Name
2-(1H-pyrrol-1-yl)aniline
Molecular Formula
C10H10N2
InChI Key
GDMZHPUPLWQIBD-UHFFFAOYSA-N
SMILES
NC1=CC=CC=C1N1C=CC=C1
Specifications
Specification SheetForm
Crystals or powder or crystalline powder
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
Description
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.
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.
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