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1-phenyl-5-({6,7,7-trifluoro-3-methyl-3-[(trimethylsilyl)oxy]-6-hepten-1-yl}sulfonyl)-1H-tetrazole

Base Information Edit
  • Chemical Name:1-phenyl-5-({6,7,7-trifluoro-3-methyl-3-[(trimethylsilyl)oxy]-6-hepten-1-yl}sulfonyl)-1H-tetrazole
  • CAS No.:1257557-46-2
  • Molecular Formula:C18H25F3N4O3SSi
  • Molecular Weight:462.568
  • Hs Code.:
  • Mol file:1257557-46-2.mol
1-phenyl-5-({6,7,7-trifluoro-3-methyl-3-[(trimethylsilyl)oxy]-6-hepten-1-yl}sulfonyl)-1H-tetrazole

Synonyms:1-phenyl-5-({6,7,7-trifluoro-3-methyl-3-[(trimethylsilyl)oxy]-6-hepten-1-yl}sulfonyl)-1H-tetrazole

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Chemical Property of 1-phenyl-5-({6,7,7-trifluoro-3-methyl-3-[(trimethylsilyl)oxy]-6-hepten-1-yl}sulfonyl)-1H-tetrazole Edit
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Technology Process of 1-phenyl-5-({6,7,7-trifluoro-3-methyl-3-[(trimethylsilyl)oxy]-6-hepten-1-yl}sulfonyl)-1H-tetrazole

There total 8 articles about 1-phenyl-5-({6,7,7-trifluoro-3-methyl-3-[(trimethylsilyl)oxy]-6-hepten-1-yl}sulfonyl)-1H-tetrazole 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 7 steps
1.1: lithium hexamethyldisilazane / tetrahydrofuran / 0.5 h / -78 °C
1.2: 0.5 h / -78 °C
2.1: lithium borohydride / tert-butyl methyl ether / 4 h / 20 °C / Cooling with ice
2.2: Cooling with ice
3.1: sodium hydroxide; p-toluenesulfonyl chloride; tetrabutylammomium bromide / toluene / 0.5 h / Cooling with ice
3.2: 60 °C
4.1: sodium hypochlorite; potassium bromide / acetonitrile; water / 2 h / Cooling with ice
5.1: diethyl ether; tetrahydrofuran / 1 h / -78 °C / Cooling with ice
6.1: dihydrogen peroxide; ammonium heptamolybdate tetrahydrate / water; methanol / 20 °C / Cooling with ice
7.1: 1H-imidazole / N,N-dimethyl-formamide / 5 h / 20 °C / Cooling with ice
With 1H-imidazole; sodium hypochlorite; lithium borohydride; ammonium heptamolybdate tetrahydrate; tetrabutylammomium bromide; dihydrogen peroxide; p-toluenesulfonyl chloride; potassium bromide; sodium hydroxide; lithium hexamethyldisilazane; In tetrahydrofuran; methanol; diethyl ether; tert-butyl methyl ether; water; N,N-dimethyl-formamide; toluene; acetonitrile;
Guidance literature:
Multi-step reaction with 6 steps
1.1: lithium borohydride / tert-butyl methyl ether / 4 h / 20 °C / Cooling with ice
1.2: Cooling with ice
2.1: sodium hydroxide; p-toluenesulfonyl chloride; tetrabutylammomium bromide / toluene / 0.5 h / Cooling with ice
2.2: 60 °C
3.1: sodium hypochlorite; potassium bromide / acetonitrile; water / 2 h / Cooling with ice
4.1: diethyl ether; tetrahydrofuran / 1 h / -78 °C / Cooling with ice
5.1: dihydrogen peroxide; ammonium heptamolybdate tetrahydrate / water; methanol / 20 °C / Cooling with ice
6.1: 1H-imidazole / N,N-dimethyl-formamide / 5 h / 20 °C / Cooling with ice
With 1H-imidazole; sodium hypochlorite; lithium borohydride; ammonium heptamolybdate tetrahydrate; tetrabutylammomium bromide; dihydrogen peroxide; p-toluenesulfonyl chloride; potassium bromide; sodium hydroxide; In tetrahydrofuran; methanol; diethyl ether; tert-butyl methyl ether; water; N,N-dimethyl-formamide; toluene; acetonitrile;
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