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1H-IMidazole, 4-broMo-1-Methyl-2-phenyl-

Base Information
  • Chemical Name:1H-IMidazole, 4-broMo-1-Methyl-2-phenyl-
  • CAS No.:86119-59-7
  • Molecular Formula:C10H9BrN2
  • Molecular Weight:237.09586
  • Hs Code.:2933299090
  • Mol file:86119-59-7.mol
1H-IMidazole, 4-broMo-1-Methyl-2-phenyl-

Synonyms:1H-IMidazole, 4-broMo-1-Methyl-2-phenyl-

Suppliers and Price of 1H-IMidazole, 4-broMo-1-Methyl-2-phenyl-
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
  • SynQuest Laboratories
  • 4-Bromo-1-methyl-2-phenyl-1H-imidazole 98.0%
  • 5 g
  • $ 1548.00
  • Chemenu
  • 4-Bromo-1-methyl-2-phenyl-1H-imidazole 95%+
  • 5g
  • $ 1394.00
  • Chemenu
  • 4-Bromo-1-methyl-2-phenyl-1H-imidazole 95%+
  • 1g
  • $ 403.00
  • Chemenu
  • 4-Bromo-1-methyl-2-phenyl-1H-imidazole 95%+
  • 250mg
  • $ 233.00
  • Chemenu
  • 4-Bromo-1-methyl-2-phenyl-1H-imidazole 95%+
  • 100mg
  • $ 121.00
Total 9 raw suppliers
Chemical Property of 1H-IMidazole, 4-broMo-1-Methyl-2-phenyl-
Chemical Property:
  • Melting Point:66-68 °C 
  • Boiling Point:360.3±34.0 °C(Predicted) 
  • PKA:3.85±0.60(Predicted) 
  • PSA:17.82000 
  • Density:1.44±0.1 g/cm3(Predicted) 
  • LogP:2.84960 
Purity/Quality:

NLT 98% *data from raw suppliers

4-Bromo-1-methyl-2-phenyl-1H-imidazole 98.0% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Uses 4-Bromo-1-methyl-2-phenyl-1H-imidazole is used in the preparation of new ligands bearing imidazole groups.
Technology Process of 1H-IMidazole, 4-broMo-1-Methyl-2-phenyl-

There total 2 articles about 1H-IMidazole, 4-broMo-1-Methyl-2-phenyl- 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 sodium hydride; In tetrahydrofuran; 1.) 0 deg C -> RT, 30 min, 2.) 0 deg C -> RT, 12 h;
DOI:10.1021/ja00354a025
Guidance literature:
Multi-step reaction with 2 steps
1: 51 percent / Na2SO3 / aq. ethanol / 46 h / Heating
2: 57 percent / NaH / tetrahydrofuran / 1.) 0 deg C -> RT, 30 min, 2.) 0 deg C -> RT, 12 h
With sodium hydride; sodium sulfite; In tetrahydrofuran; ethanol;
DOI:10.1021/ja00354a025
Guidance literature:
With n-butyllithium; In tetrahydrofuran; hexane; 1.) -78 deg C, 30 min, 2.) -78 deg C -> -40 deg C, 30 min;
DOI:10.1021/ja00354a025
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