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N-[1-cyano-1-methyl-2-(5-cyano-2-{2-chloro-4-trifluoromethoxy-phenoxy}-phenoxy)-ethyl]-4-trifluoromethylsulfonylbenzamide

Base Information
  • Chemical Name:N-[1-cyano-1-methyl-2-(5-cyano-2-{2-chloro-4-trifluoromethoxy-phenoxy}-phenoxy)-ethyl]-4-trifluoromethylsulfonylbenzamide
  • CAS No.:1309111-23-6
  • Molecular Formula:C26H16ClF6N3O6S
  • Molecular Weight:647.939
  • Hs Code.:
N-[1-cyano-1-methyl-2-(5-cyano-2-{2-chloro-4-trifluoromethoxy-phenoxy}-phenoxy)-ethyl]-4-trifluoromethylsulfonylbenzamide

Synonyms:N-[1-cyano-1-methyl-2-(5-cyano-2-{2-chloro-4-trifluoromethoxy-phenoxy}-phenoxy)-ethyl]-4-trifluoromethylsulfonylbenzamide

Suppliers and Price of N-[1-cyano-1-methyl-2-(5-cyano-2-{2-chloro-4-trifluoromethoxy-phenoxy}-phenoxy)-ethyl]-4-trifluoromethylsulfonylbenzamide
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of N-[1-cyano-1-methyl-2-(5-cyano-2-{2-chloro-4-trifluoromethoxy-phenoxy}-phenoxy)-ethyl]-4-trifluoromethylsulfonylbenzamide
Chemical Property:
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MSDS Files:
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Technology Process of N-[1-cyano-1-methyl-2-(5-cyano-2-{2-chloro-4-trifluoromethoxy-phenoxy}-phenoxy)-ethyl]-4-trifluoromethylsulfonylbenzamide

There total 6 articles about N-[1-cyano-1-methyl-2-(5-cyano-2-{2-chloro-4-trifluoromethoxy-phenoxy}-phenoxy)-ethyl]-4-trifluoromethylsulfonylbenzamide 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 6 steps
1.1: caesium carbonate / N,N-dimethyl-formamide / 16 h / 120 °C
2.1: boron tribromide / dichloromethane / 20.5 h / 10 - 20 °C
2.2: Cooling with ice
3.1: potassium carbonate; potassium iodide / acetone / 4 h / Reflux
4.1: ammonia; ammonium chloride / ethanol; water / 16 h / 20 °C
5.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 20 h / 20 °C
6.1: sodium periodate / ruthenium trichloride / tetrachloromethane; acetonitrile; water / 1.5 h / 20 °C
With sodium periodate; ammonia; boron tribromide; potassium carbonate; ammonium chloride; caesium carbonate; N-ethyl-N,N-diisopropylamine; potassium iodide; ruthenium trichloride; In tetrachloromethane; ethanol; dichloromethane; water; N,N-dimethyl-formamide; acetone; acetonitrile;
Guidance literature:
Multi-step reaction with 6 steps
1.1: caesium carbonate / N,N-dimethyl-formamide / 16 h / 120 °C
2.1: boron tribromide / dichloromethane / 20.5 h / 10 - 20 °C
2.2: Cooling with ice
3.1: potassium carbonate; potassium iodide / acetone / 4 h / Reflux
4.1: ammonia; ammonium chloride / ethanol; water / 16 h / 20 °C
5.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 20 h / 20 °C
6.1: sodium periodate / ruthenium trichloride / tetrachloromethane; acetonitrile; water / 1.5 h / 20 °C
With sodium periodate; ammonia; boron tribromide; potassium carbonate; ammonium chloride; caesium carbonate; N-ethyl-N,N-diisopropylamine; potassium iodide; ruthenium trichloride; In tetrachloromethane; ethanol; dichloromethane; water; N,N-dimethyl-formamide; acetone; acetonitrile;
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