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tert-Butyl-((5Z,8Z,11Z,14Z)-5,6-difluoro-icosa-5,8,11,14-tetraenyloxy)-diphenyl-silane

Base Information
  • Chemical Name:tert-Butyl-((5Z,8Z,11Z,14Z)-5,6-difluoro-icosa-5,8,11,14-tetraenyloxy)-diphenyl-silane
  • CAS No.:179872-59-4
  • Molecular Formula:C36H50F2OSi
  • Molecular Weight:564.875
  • Hs Code.:
tert-Butyl-((5Z,8Z,11Z,14Z)-5,6-difluoro-icosa-5,8,11,14-tetraenyloxy)-diphenyl-silane

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Chemical Property of tert-Butyl-((5Z,8Z,11Z,14Z)-5,6-difluoro-icosa-5,8,11,14-tetraenyloxy)-diphenyl-silane
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Technology Process of tert-Butyl-((5Z,8Z,11Z,14Z)-5,6-difluoro-icosa-5,8,11,14-tetraenyloxy)-diphenyl-silane

There total 9 articles about tert-Butyl-((5Z,8Z,11Z,14Z)-5,6-difluoro-icosa-5,8,11,14-tetraenyloxy)-diphenyl-silane 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,N,N-hexamethylphosphoric triamide; n-butyllithium; In tetrahydrofuran; -78 deg C, 30 min; 0 deg C, 1 h; 30 min, RT;
DOI:10.1016/0040-4039(96)00976-8
Guidance literature:
Multi-step reaction with 10 steps
1: 75 percent / MeDAST / CH2Cl2 / 48 h / Ambient temperature
2: 91 percent / (n-Bu)3SnH / AIBN / toluene / Heating
3: 92 percent / H2 / Pearlman's catalyst / ethyl acetate / 6 h / 760 Torr
4: 96 percent / Et3N, DMAP / CH2Cl2 / Ambient temperature
5: 66 percent / <(CH3)3Si>2NNa / tetrahydrofuran / 1 h / Ambient temperature
6: 94 percent / DIBAL / hexane; diethyl ether / 1 h
7: 96 percent / 1-bromo-N,N-2-trimethylpropenylamine / CH2Cl2 / 0.25 h / 0 °C
8: tetrahydrofuran / 12 h / Ambient temperature
9: 1.) Amberlyst A21, HCl form; 2.) Amberlyst A26, Cl(1-) / 1.5 h
10: 23 percent / n-BuLi, HMPTA / tetrahydrofuran / -78 deg C, 30 min; 0 deg C, 1 h; 30 min, RT
With hydrogenchloride; N,N,N,N,N,N-hexamethylphosphoric triamide; dmap; n-butyllithium; amberlyst A21; dimethylaminosulphur trifluoride; 1-bromo-N,N,2-trimethyl-1-propen-1-amine; chloride; hydrogen; tri-n-butyl-tin hydride; sodium hexamethyldisilazane; diisobutylaluminium hydride; triethylamine; Amberlyst A26; palladium dihydroxide; 2,2'-azobis(isobutyronitrile); In tetrahydrofuran; diethyl ether; hexane; dichloromethane; ethyl acetate; toluene;
DOI:10.1016/0040-4039(96)00976-8
Guidance literature:
Multi-step reaction with 9 steps
1: 91 percent / (n-Bu)3SnH / AIBN / toluene / Heating
2: 92 percent / H2 / Pearlman's catalyst / ethyl acetate / 6 h / 760 Torr
3: 96 percent / Et3N, DMAP / CH2Cl2 / Ambient temperature
4: 66 percent / <(CH3)3Si>2NNa / tetrahydrofuran / 1 h / Ambient temperature
5: 94 percent / DIBAL / hexane; diethyl ether / 1 h
6: 96 percent / 1-bromo-N,N-2-trimethylpropenylamine / CH2Cl2 / 0.25 h / 0 °C
7: tetrahydrofuran / 12 h / Ambient temperature
8: 1.) Amberlyst A21, HCl form; 2.) Amberlyst A26, Cl(1-) / 1.5 h
9: 23 percent / n-BuLi, HMPTA / tetrahydrofuran / -78 deg C, 30 min; 0 deg C, 1 h; 30 min, RT
With hydrogenchloride; N,N,N,N,N,N-hexamethylphosphoric triamide; dmap; n-butyllithium; amberlyst A21; 1-bromo-N,N,2-trimethyl-1-propen-1-amine; chloride; hydrogen; tri-n-butyl-tin hydride; sodium hexamethyldisilazane; diisobutylaluminium hydride; triethylamine; Amberlyst A26; palladium dihydroxide; 2,2'-azobis(isobutyronitrile); In tetrahydrofuran; diethyl ether; hexane; dichloromethane; ethyl acetate; toluene;
DOI:10.1016/0040-4039(96)00976-8
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