ChemicalBook--->CAS DataBase List--->10040-96-7

10040-96-7

10040-96-7 Structure

10040-96-7 Structure
IdentificationMore
[Name]

1-(4-BROMOPHENYL)IMIDAZOLE
[CAS]

10040-96-7
[Synonyms]

1-(4-BROMOPHENYL)IMIDAZOLE
1-(4-Bromophenyl)-1H-imidazole
[Molecular Formula]

C9H7BrN2
[MDL Number]

MFCD00060489
[Molecular Weight]

223.07
[MOL File]

10040-96-7.mol
Chemical PropertiesBack Directory
[Melting point ]

118-120°C
[Boiling point ]

323.4±25.0 °C(Predicted)
[density ]

1.50±0.1 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[form ]

powder to crystal
[pka]

5.24±0.10(Predicted)
[color ]

White to Light yellow
[CAS DataBase Reference]

10040-96-7(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319
[Precautionary statements ]

P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
[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 .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
[HazardClass ]

IRRITANT
[HS Code ]

2933299090
Spectrum DetailBack Directory
[Spectrum Detail]

1-(4-BROMOPHENYL)IMIDAZOLE(10040-96-7)1HNMR
Hazard InformationBack Directory
[Synthesis]

Imidazole

288-32-4

4-Bromophenylboronic acid

5467-74-3

1-(4-BROMOPHENYL)IMIDAZOLE

10040-96-7

A magnetic stirrer, imidazole (59 mg, 0.5 mmol), 4-bromophenylboronic acid (1.0 mmol), cuprous sulfide (4 mg, 0.025 mmol), and methanol (2 mL) were added to a 10 mL round bottom flask followed by N,N,N',N'-tetramethylethylenediamine (TMEDA, 0.075 mL, 0.5 mmol). The flask was sealed with a rubber septum and an 18-gauge needle was inserted to allow air to enter the reaction system while preventing contamination of the mixture. The reaction mixture was stirred at 400 to 600 rpm for an appropriate time. After completion of the reaction, the reaction mixture was extracted with ethyl acetate (2 x 15 mL). The organic layers were combined and washed with saturated aqueous ethylenediaminetetraacetic acid disodium salt solution (15 mL), followed by drying with anhydrous sodium sulfate. The solvent was removed by concentration under reduced pressure and the residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate) to afford the target product 1-(4-bromophenyl)imidazole. The structure of the product was characterized by 1H NMR, 13C NMR, high resolution mass spectrometry (HRMS) and melting point (if solid).

[References]

[1] Synthesis, 2008, # 5, p. 795 - 799
[2] Tetrahedron, 2018, vol. 74, # 5, p. 606 - 617
[3] Green Chemistry, 2018, vol. 20, # 21, p. 4891 - 4900
[4] Catalysis Communications, 2018, vol. 109, p. 38 - 42
[5] Tetrahedron, 2012, vol. 68, # 38, p. 7794 - 7798
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