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ChemicalBook--->CAS DataBase List--->484-47-9

484-47-9

484-47-9 Structure

484-47-9 Structure
IdentificationMore
[Name]

2,4,5-TRIPHENYLIMIDAZOLE
[CAS]

484-47-9
[Synonyms]

2,4,5-TRIPHENYLIMIDAZOLE
LOPHINE
2,4,5-triphenyl-1h-imidazol
2,4,5-triphenyl-1H-Imidazole
2,4,5-triphenyl-imidazol
2,4,5-triphenylimidazole (Lophine)
1H-Imidazole,2,4,5-triphenyl-
Lophin
[EINECS(EC#)]

207-606-6
[Molecular Formula]

C21H16N2
[MDL Number]

MFCD00005187
[Molecular Weight]

296.37
[MOL File]

484-47-9.mol
Chemical PropertiesBack Directory
[Appearance]

OFF-WHITE POWDER
[Melting point ]

274-278 °C (lit.)
[Boiling point ]

427.96°C (rough estimate)
[density ]

1.0874 (rough estimate)
[refractive index ]

1.8000 (estimate)
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

powder to crystal
[pka]

11.66±0.10(Predicted)
[color ]

White to Orange to Green
[Water Solubility ]

Soluble in methanol. Insoluble in water.
[λmax]

300nm(EtOH)(lit.)
[BRN ]

236652
[InChI]

InChI=1S/C21H16N2/c1-4-10-16(11-5-1)19-20(17-12-6-2-7-13-17)23-21(22-19)18-14-8-3-9-15-18/h1-15H,(H,22,23)
[InChIKey]

RNIPJYFZGXJSDD-UHFFFAOYSA-N
[SMILES]

C1(C2=CC=CC=C2)NC(C2=CC=CC=C2)=C(C2=CC=CC=C2)N=1
[CAS DataBase Reference]

484-47-9(CAS DataBase Reference)
[EPA Substance Registry System]

1H-Imidazole, 2,4,5-triphenyl- (484-47-9)
Safety DataBack Directory
[Safety Statements ]

S22:Do not breathe dust .
S24/25:Avoid contact with skin and eyes .
[WGK Germany ]

3
[RTECS ]

NI8710000
[TSCA ]

Yes
[HS Code ]

29349990
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Ethanol-->Benzaldehyde-->Benzil-->triphenyloxazole-->1H-1,2,4-Triazole-3-thiol-->2-(2-Chlorophenyl)-4,5-diphenylimidazole-->BENZAMIDINE-->2,2'-Bis(2-chlorophenyl)-4,4',5,5'-tetraphenyl-1,2'-biimidazole-->Diphenylacetylene-->2-Phenylacetophenone-->Urea-->Benzonitrile-->BENZAMIDOXIME HYDROCHLORIDE
Hazard InformationBack Directory
[Chemical Properties]

OFF-WHITE POWDER
[Uses]

2,4,5-Triphenylimidazole is used in the synthesis of fluorescent diarylethenes and nanowires of 2,4,5-triphenylimidazole, which finds application as single wire active optical waveguides and optically driven ultraviolet lasers.
[Preparation]

2,4,5-triphenylimidazole was synthesized by reaction between ammonia, benzaldehyde and benzoin: Benzoin (1) ( 5 g, 0.023 M) was reacted with benzaldehyde (5 mL, 0.05 mol) (2) in presence of ammonia (3) and refluxed for 4 h and the resulting mixture was cooled, filtered to get 2,4,5-triphenylimidazole (4).
Synthesis of 2,4,5-Triphenylimidazoles Novel Mannich Bases as Potential Antiinflammatory and Analgesic Agents
DOI: 10.3923/crc.2012.99.109
Spectrum DetailBack Directory
[Spectrum Detail]

2,4,5-TRIPHENYLIMIDAZOLE(484-47-9)1HNMR
2,4,5-TRIPHENYLIMIDAZOLE(484-47-9)13CNMR
2,4,5-TRIPHENYLIMIDAZOLE(484-47-9)IR1
2,4,5-TRIPHENYLIMIDAZOLE(484-47-9)IR2
2,4,5-TRIPHENYLIMIDAZOLE(484-47-9)Raman
2,4,5-TRIPHENYLIMIDAZOLE(484-47-9)ESR
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

2,4,5-Triphenylimidazole, 98%(484-47-9)
[Alfa Aesar]

2,4,5-Triphenylimidazole, 97%(484-47-9)
[Sigma Aldrich]

484-47-9(sigmaaldrich)
[TCI AMERICA]

2,4,5-Triphenylimidazole,>98.0%(LC)(T)(484-47-9)
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