Basic information Safety Supplier Related

1-(2-AMINOPHENYL)PYRROLE

Basic information Safety Supplier Related

1-(2-AMINOPHENYL)PYRROLE Basic information

Product Name:
1-(2-AMINOPHENYL)PYRROLE
Synonyms:
  • 1-(o-Aminophenyl)-1H-pyrrole
  • 2-(1H-Pyrrol-1-yl)benzenamine
  • [2-(1H-Pyrrol-1-yl)phenyl]amine
  • (2-pyrrol-1-ylphenyl)amine
  • 2-pyrrol-1-ylaniline
  • Benzenamine, 2-(1H-pyrrol-1-yl)-
  • N-(2-Aminophenyl)pyrrole
  • 2-(1H-PYRROL-1-YL)ANILINE
CAS:
6025-60-1
MF:
C10H10N2
MW:
158.2
EINECS:
227-884-2
Product Categories:
  • Building Blocks
  • Heterocyclic Building Blocks
  • Pyrroles
Mol File:
6025-60-1.mol
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1-(2-AMINOPHENYL)PYRROLE Chemical Properties

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
pka
2.09±0.10(Predicted)
Water Solubility 
Insoluble in water.
BRN 
1307631
CAS DataBase Reference
6025-60-1(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xn
Risk Statements 
20/21/22-36/37/38
Safety Statements 
26-36
WGK Germany 
3
PackingGroup 
III
HS Code 
29339980

MSDS

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1-(2-AMINOPHENYL)PYRROLE Usage And Synthesis

Chemical Properties

LIGHT BEIGE TO BROWN CRYSTAL. POWDER AND NEEDLES

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.

Uses

1-(2-Aminophenyl)pyrrole was used in the synthesis of 4-substituted pyrrolo[1,2-a]quinoxaline derivatives.

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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