4-(4-Fluorophenyl)-1H-imidazole

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4-(4-Fluorophenyl)-1H-imidazole Basic information
Uses
Product Name:4-(4-Fluorophenyl)-1H-imidazole
Synonyms:5-(4-Fluorophenyl)-3H-imidazole;4-(4-Fluorophenyl)iMidazole, 97%;JR-9093, 4-(4-Fluorophenyl)-1H-imidazole, 97%;1H-Imidazole, 5-(4-fluorophenyl)-;4-(4-Fluorophenyl)imidazole, 97%,;4-(4-Fluorophenyl)-1H-imidazole;4-(4-Fluorophenyl)imidazole;4-(4-Fluorophenyl)-1H-imidazole
CAS:65020-70-4
MF:C9H7FN2
MW:162.16
EINECS:
Product Categories:Heterocyclic Compounds
Mol File:65020-70-4.mol
4-(4-Fluorophenyl)-1H-imidazole Structure
4-(4-Fluorophenyl)-1H-imidazole Chemical Properties
Melting point 124-129 °C
form solid
InChI1S/C9H7FN2/c10-8-3-1-7(2-4-8)9-5-11-6-12-9/h1-6H,(H,11,12)
InChIKeyQYDAFWKRBZYBOB-UHFFFAOYSA-N
SMILESFc1ccc(cc1)-c2c[nH]cn2
Safety Information
Hazard Codes Xn
Risk Statements 22-41
Safety Statements 26
WGK Germany 3
HS Code 2933299090
Storage Class11 - Combustible Solids
Hazard ClassificationsAcute Tox. 4 Oral
Eye Dam. 1
MSDS Information
4-(4-Fluorophenyl)-1H-imidazole Usage And Synthesis
Uses4-(4-Fluorophenyl)-1H-imidazolium is an imidazolium heterocyclic derivative that can be used as an intermediate in pharmaceutical and chemical synthesis.
Synthesis

A mixture of 2-bromo-1-(4-fluorophenyl)ethanone (10.9 g, 50 mmol) and formamide (14 mL, 350 mmol) was stirred at 170 C and under nitrogen for 4 hours. The reaction mixture was cooled and mixed with ethyl acetate (40 mL). Saturated aqueous sodium bicarbonate (50 mL) was carefully added while the mixture was cooled in an ice water bath. The aqueous layer was separated and extracted with ethyl acetate (2 x 40mL). The combined organic solutions were washed with water (30 mL) and brine (30 mL), dried (Na2SO 4) and concentrated.  Rapid chromatography on silica gel (10-100% hexane solution of ethyl acetate) yielded 4-(4-fluorophenyl)-1H-imidazole (3.46 g, 21 mmol, 43% yield) as a solid.

4-(4-Fluorophenyl)-1H-imidazole Preparation Products And Raw materials
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