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1-PHENYL-1H-BENZOIMIDAZOLE

Base Information
  • Chemical Name:1-PHENYL-1H-BENZOIMIDAZOLE
  • CAS No.:2622-60-8
  • Molecular Formula:C13H10N2
  • Molecular Weight:194.236
  • Hs Code.:
  • Mol file:2622-60-8.mol
1-PHENYL-1H-BENZOIMIDAZOLE

Synonyms:Benzimidazole,1-phenyl- (6CI,7CI,8CI);1-Phenyl-1H-benzimidazole;1-Phenylbenzimidazole;N-Phenylbenzimidazole;

Suppliers and Price of 1-PHENYL-1H-BENZOIMIDAZOLE
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • 1-phenyl-1h-benzo[d]imidazole
  • 500mg
  • $ 285.00
  • Matrix Scientific
  • 1-Phenyl-1H-benzoimidazole 95%
  • 1g
  • $ 500.00
  • Matrix Scientific
  • 1-Phenyl-1H-benzoimidazole 95%
  • 5g
  • $ 975.00
  • Crysdot
  • 1-Phenyl-1H-benzo[d]imidazole 98%
  • 5g
  • $ 554.00
  • Crysdot
  • 1-Phenyl-1H-benzo[d]imidazole 98%
  • 1g
  • $ 238.00
  • Crysdot
  • 1-Phenyl-1H-benzo[d]imidazole 98%
  • 10g
  • $ 842.00
  • Chemenu
  • 1-phenyl-1H-benzo[d]imidazole 98%
  • 10g
  • $ 795.00
  • American Custom Chemicals Corporation
  • 1-PHENYL-1H-BENZOIMIDAZOLE 95.00%
  • 1G
  • $ 945.95
  • Alichem
  • 1-Phenyl-1H-benzo[d]imidazole
  • 1g
  • $ 190.16
  • Alichem
  • 1-Phenyl-1H-benzo[d]imidazole
  • 5g
  • $ 443.81
Total 26 raw suppliers
Chemical Property of 1-PHENYL-1H-BENZOIMIDAZOLE
Chemical Property:
  • Vapor Pressure:1.86E-05mmHg at 25°C 
  • Melting Point:98℃ 
  • Refractive Index:1.638 
  • Boiling Point:363 °C at 760 mmHg 
  • PKA:4.42±0.10(Predicted) 
  • Flash Point:173.3 °C 
  • PSA:17.82000 
  • Density:1.13 g/cm3 
  • LogP:3.02550 
  • Storage Temp.:Sealed in dry,Room Temperature 
Purity/Quality:

97% *data from raw suppliers

1-phenyl-1h-benzo[d]imidazole *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Uses 1-phenyl-1h-benzo[d]imidazole is a useful research chemical.
Technology Process of 1-PHENYL-1H-BENZOIMIDAZOLE

There total 57 articles about 1-PHENYL-1H-BENZOIMIDAZOLE 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:
Guidance literature:
With N,N,N,N,-tetramethylethylenediamine; oxygen; copper(II) nitrate; In methanol; at 20 ℃; for 24h; under 760.051 Torr;
DOI:10.1002/adsc.200800730
Guidance literature:
With copper(l) iodide; potassium carbonate; heptakis(6-amino-6-deoxy)-β-cyclodextrin; In dimethyl sulfoxide; at 110 ℃; for 24h; Sealed tube;
DOI:10.1021/jo801811w
Guidance literature:
With copper(l) iodide; potassium carbonate; L-proline; PS[DMVBIM][Pro]; In dimethyl sulfoxide; at 120 ℃; for 60h;
DOI:10.1021/ja073633n
Refernces

FREE-RADICAL HYDROXYMETHYLATION OF BENZIMIDAZOLE

10.1007/BF00506621

The research investigates the free-radical hydroxymethylation of benzimidazole derivatives and the condensation of 3,4-dicyano-5-aminopyrazole with ethyl orthoformate. In the hydroxymethylation study, benzimidazole derivatives such as 1-methylbenzimidazole and 1-phenylbenzimidazole were subjected to free-radical hydroxymethylation using ammonium persulfate in methanol and sulfuric acid, with silver ions as a catalyst to enhance yields. The study found that benzimidazole displayed lower activity than quinoline in the addition of the hydroxymethyl radical, and the yields of hydroxymethylation products were influenced by the ability of intermediate benzimidazolium cation radicals to undergo oxidation. In the condensation study, 3,4-dicyano-5-aminopyrazole was reacted with ethyl orthoformate under different conditions to produce compounds like N-ethyl-3,4-dicyano-5-ethoxymethyleneaminopyrazole and 3,4-dicyano-5-ethoxymethyleneaminopyrazole. The formation of these products and their subsequent conversion to pyrazolo[3,4-d]pyrimidines using a methanol solution of ammonia were also explored.

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