1-(2-AMINOPHENYL)PYRROLE
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
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)
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
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
- Language:English Provider:ALFA
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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1-(2-AMINOPHENYL)PYRROLE(6025-60-1)Related Product Information
- 1-(2-NITROPHENYL)PYRROLE
- 1-(2-AMINOPHENYL)PYRROLE
- 1-(4-AMINOPHENYL)PYRROLE
- 1-(3-AMINOPHENYL)PYRROLE
- Pyrrole
- 1-(2-NITROPHENYL)-1H-PYRROLE-2-CARBALDEHYDE
- 9-[2-NITRO-4-(TRIFLUOROMETHYL)PHENYL]-9H-CARBAZOLE
- pyrrolo[1,2-a]quinoxaline
- PYRROLO[1,2-A]QUINOXALIN-4(5H)-ONE
- 5-METHOXY-2-(1H-PYRROL-1-YL)ANILINE
- 1-[2,3,4,5,6-PENTA(1H-PYRROL-1-YL)PHENYL]-1H-PYRROLE
- 5-METHYL-2-(1H-PYRROL-1-YL)ANILINE
- 1-[2-NITRO-4-(TRIFLUOROMETHYL)PHENYL]-1H-PYRROLE
- 7-Trifluoromethyl-4-(4-methyl-1-piperazinyl)pyrrolo-[1,2-a]quinoxaline maleate salt
- 2-(1H-PYRROL-1-YL)-5-(TRIFLUOROMETHYL)ANILINE
- 2,2,2-TRICHLORO-1-[1-(2-NITROPHENYL)-1H-PYRROL-2-YL]ETHAN-1-ONE
- 4-CHLOROPYRROLO[1,2-A]QUINOXALINE
- 1-Boc-3-(3-Aminophenyl)Pyrrolidine