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2-(2-pyridyl)-4-phenyl-6-(4-trifluoromethylphenyl)phosphinine-P,N-tungsten tetracarbonyl

Base Information Edit
  • Chemical Name:2-(2-pyridyl)-4-phenyl-6-(4-trifluoromethylphenyl)phosphinine-P,N-tungsten tetracarbonyl
  • CAS No.:1616765-12-8
  • Molecular Formula:C27H15F3NO4PW
  • Molecular Weight:689.239
  • Hs Code.:
  • Mol file:1616765-12-8.mol
2-(2-pyridyl)-4-phenyl-6-(4-trifluoromethylphenyl)phosphinine-P,N-tungsten tetracarbonyl

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Suppliers and Price of 2-(2-pyridyl)-4-phenyl-6-(4-trifluoromethylphenyl)phosphinine-P,N-tungsten tetracarbonyl
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 2-(2-pyridyl)-4-phenyl-6-(4-trifluoromethylphenyl)phosphinine-P,N-tungsten tetracarbonyl Edit
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Technology Process of 2-(2-pyridyl)-4-phenyl-6-(4-trifluoromethylphenyl)phosphinine-P,N-tungsten tetracarbonyl

There total 7 articles about 2-(2-pyridyl)-4-phenyl-6-(4-trifluoromethylphenyl)phosphinine-P,N-tungsten tetracarbonyl 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:
Multi-step reaction with 4 steps
1: sodium hydroxide / 0.17 h / Milling
2: 3 h / 80 °C / Inert atmosphere
3: Tris(trimethylsilyl)phosphane / acetonitrile / 6 h / 85 °C / Inert atmosphere
4: tetrahydrofuran-d8 / UV-irradiation
With Tris(trimethylsilyl)phosphane; sodium hydroxide; In tetrahydrofuran-d8; acetonitrile;
DOI:10.1039/c4cc03469d
Guidance literature:
Multi-step reaction with 2 steps
1: Tris(trimethylsilyl)phosphane / acetonitrile / 6 h / 85 °C / Inert atmosphere
2: tetrahydrofuran-d8 / UV-irradiation
With Tris(trimethylsilyl)phosphane; In tetrahydrofuran-d8; acetonitrile;
DOI:10.1039/c4cc03469d
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