ChemicalBook--->CAS DataBase List--->219814-29-6

219814-29-6

219814-29-6 Structure

219814-29-6 Structure
IdentificationBack Directory
[Name]

2,5-Dibromo-4-methylimidazole
[CAS]

219814-29-6
[Synonyms]

2,5-DIBROMO-4-METHYLIMIDAZOLE
2,5-Dibromo-4-methyl-1H-imidazole
2,4-dibromo-5-methyl-1H-imidazole
1H-Imidazole, 2,5-dibromo-4-methyl-
1H-Imidazole, 2,4-dibromo-5-methyl-
[Molecular Formula]

C4H4Br2N2
[MDL Number]

MFCD02179519
[MOL File]

219814-29-6.mol
[Molecular Weight]

239.9
Chemical PropertiesBack Directory
[Boiling point ]

343.1±34.0 °C(Predicted)
[density ]

2.188±0.06 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[pka]

9.47±0.10(Predicted)
[Appearance]

Off-white to light yellow Solid
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[Risk Statements ]

36/37/38
[Safety Statements ]

26-36/37/39
[HS Code ]

2933299090
Spectrum DetailBack Directory
[Spectrum Detail]

2,5-Dibromo-4-methylimidazole(219814-29-6)1HNMR
Hazard InformationBack Directory
[Synthesis]

4-Methylimidazole

822-36-6

2,5-Dibromo-4-methylimidazole

219814-29-6

General procedure for the synthesis of 2,5-dibromo-4-methylimidazole from 4-methylimidazole: 4-methylimidazole (3.4 g, 40 mmol) was dissolved in tetrahydrofuran (THF, 50 mL) at room temperature. Subsequently, N-bromosuccinimide (NBS, 14 g, 80 mmol) was added to this solution. The reaction mixture was stirred for 1 hour. After completion of the reaction, the solvent was removed by distillation under reduced pressure. The crude product was purified by silica gel column chromatography (eluent ratio: petroleum ether (PE):ethyl acetate (EA) = 2:1) to afford 2,5-dibromo-4-methylimidazole (9.6 g, 99% yield) as a white solid. Mass spectrometry (ESI-MS) analysis showed: m/z 239.0 [M + H]+.

[References]

[1] Patent: WO2015/26792, 2015, A1. Location in patent: Paragraph 0229
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