ChemicalBook--->CAS DataBase List--->107302-22-7

107302-22-7

107302-22-7 Structure

107302-22-7 Structure
IdentificationMore
[Name]

1-(3-Bromophenyl)-1H-pyrrole
[CAS]

107302-22-7
[Synonyms]

1-(3-BROMOPHENYL)-1H-PYRROLE
BUTTPARK 96\50-04
1-(3-Bromophenyl)-1h-pyrrole, 95+%
[Molecular Formula]

C10H8BrN
[MDL Number]

MFCD02665243
[Molecular Weight]

222.08
[MOL File]

107302-22-7.mol
Chemical PropertiesBack Directory
[Melting point ]

63 °C
[Boiling point ]

294.9±23.0 °C(Predicted)
[density ]

1.38±0.1 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

-5.74±0.70(Predicted)
[CAS DataBase Reference]

107302-22-7(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S37/39:Wear suitable gloves and eye/face protection .
[Hazard Note ]

Irittant
[HazardClass ]

IRRITANT
[HS Code ]

2933998090
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

1-(3-bromophenyl)-1H-pyrrole(107302-22-7)
Hazard InformationBack Directory
[Synthesis]

2,5-Dimethoxytetrahydrofuran

696-59-3

3-Bromoaniline

591-19-5

1-(3-Bromophenyl)-1H-pyrrole

107302-22-7

General procedure: m-Bromoaniline (1 mmol), 2,5-dimethoxytetrahydrofuran (1.1 mmol) and L-(+)-tartaric acid-chlorocholinesterase DES (1.5 g) were added to a 50 mL round-bottomed flask and the reaction mixture was stirred at 90°C. The reaction was carried out by thin-layer chromatography (TLC). The reaction process was monitored by thin layer chromatography (TLC). After completion of the reaction, the mixture was cooled to room temperature and the target product 1-(3-bromophenyl)-1H-pyrrole was extracted with ethyl acetate. After evaporation of the solvent, the residue was purified by silica gel column chromatography to give the pure product.DES was dried under vacuum and reused for the next cycle.

[References]

[1] Asian Journal of Chemistry, 2013, vol. 25, # 1, p. 501 - 504
[2] Journal of Molecular Liquids, 2014, vol. 198, p. 259 - 262,4
[3] Applied Catalysis A: General, 2013, vol. 457, p. 34 - 41
[4] Journal of the Chemical Society. Perkin Transactions 1, 2001, # 9, p. 1039 - 1043
[5] Journal of Heterocyclic Chemistry, 2000, vol. 37, # 1, p. 15 - 24
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