1,5-Diphenylimidazole

Base Information

• Chemical Name: 1,5-Diphenylimidazole
• CAS No.: 61278-58-8
• Molecular Formula: C15H12N2
• Molecular Weight: 220.274
• DSSTox Substance ID: DTXSID50396187
• Nikkaji Number: J792.988I
• Wikidata: Q82196760
• ChEMBL ID: CHEMBL1357891

Synonyms:1,5-Diphenyl-1H-imidazole;1,5-diphenylimidazole;1H-Imidazole, 1,5-diphenyl-;61278-58-8;MLS001240962;CHEMBL1357891;SCHEMBL12676747;DTXSID50396187;JBLLBGIUSCXVSG-UHFFFAOYSA-N;HMS2216E03;HMS3337A03;SMR000841295

Chemical Property of 1,5-Diphenylimidazole

Chemical Property:

• XLogP3: 3.3
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 2
• Exact Mass: 220.100048391
• Heavy Atom Count: 17
• Complexity: 229

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)C2=CN=CN2C3=CC=CC=C3

Technology Process of 1,5-Diphenylimidazole

There total 7 articles about 1,5-Diphenylimidazole which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 85.0%

1-(isocyanomethyl)-1H-benzo[d][1,2,3]triazole (87022-42-2) + benzylidene phenylamine (538-51-2) → 1,5-Diphenylimidazole (61278-58-8)

Guidance literature:

With potassium tert-butylate; In dimethyl sulfoxide; at 75 ℃;

Reference yield: 41.0%

1-phenylimidazole (7164-98-9) + iodobenzene (591-50-4) → 1,2,5-triphenyl-1H-imidazole (19278-31-0) + 1,5-Diphenylimidazole (61278-58-8) + 1,2-diphenylimidazole (52179-66-5)

Guidance literature:

With triphenyl-arsane; cesium fluoride; palladium diacetate; In N,N-dimethyl-formamide; at 140 ℃; for 23h;

DOI:10.1021/jo050274a

Reference yield: 18.0%

[(p-methylphenyl)sulfonylmethyl]isonitrile (38622-91-2,36635-61-7) + (E)-N-benzylidenebenzenamine (1750-36-3,33993-35-0,538-51-2,137431-97-1,137432-04-3) → 1,5-Diphenylimidazole (61278-58-8)

Guidance literature:

With sodium t-butanolate; In tetrahydrofuran; at 20 ℃; for 120h;

upstream raw materials:

1-(isocyanomethyl)-1H-benzo[d][1,2,3]triazole

benzylidene phenylamine

iodobenzene

4-Phenylimidazole

Downstream raw materials:

2-<<2-(dimethylamino)benzyl>thio>-1,5-diphenylimidazole

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