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

Catalog Number p-7044514
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Quantity:
1 g
5 g
This item is not returnable. View return policy
To receive the discount customers must purchase three of the same product at list price in a single order to receive 33.33% discount. There is no limit to the multiples of 3 that customers can buy. Use promo code ”21615” to get your promotional price
6025-60-1
C10H10N2
158.204
MFCD00005344
GDMZHPUPLWQIBD-UHFFFAOYSA-N
1-2-aminophenyl pyrrole, 2-1h-pyrrol-1-yl aniline, n-2-aminophenyl pyrrole, 2-1h-pyrrol-1-yl phenyl amine, 1-2-aminophenyl-1h-pyrrole, 2-1-pyrrolyl aniline, benzenamine, 2-1h-pyrrol-1-yl, 2-pyrrolylphenylamine, 2-pyrrol-1-yl aniline, acmc-20apd3
80123
2-pyrrol-1-ylaniline
C1=CC=C(C(=C1)N)N2C=CC=C2
This item is not returnable. View return policy
To receive the discount customers must purchase three of the same product at list price in a single order to receive 33.33% discount. There is no limit to the multiples of 3 that customers can buy. Use promo code ”21615” to get your promotional price
6025-60-1
C10H10N2
158.204
MFCD00005344
GDMZHPUPLWQIBD-UHFFFAOYSA-N
1-2-aminophenyl pyrrole, 2-1h-pyrrol-1-yl aniline, n-2-aminophenyl pyrrole, 2-1h-pyrrol-1-yl phenyl amine, 1-2-aminophenyl-1h-pyrrole, 2-1-pyrrolyl aniline, benzenamine, 2-1h-pyrrol-1-yl, 2-pyrrolylphenylamine, 2-pyrrol-1-yl aniline, acmc-20apd3
80123
2-pyrrol-1-ylaniline
C1=CC=C(C(=C1)N)N2C=CC=C2

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.
TRUSTED_SUSTAINABILITY
Melting Point 93°C to 94°C
Quantity 1 g
Beilstein 1307631
Solubility Information Insoluble in water.
Formula Weight 158.2
Percent Purity ≥98%
Chemical Name or Material 1-(2-Aminophenyl)pyrrole

RUO – Research Use Only

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