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(2R,4S,7S)-11-(tert-butyldimethylsilanyloxy)-3-(tert-butyldiphenylsilanyloxy)-7-hydroxy-5-(4-methoxybenzyloxy)-8,8-dimethyl-9-methyleneundecanethioic acid S-tert-butyl ester

Base Information
  • Chemical Name:(2R,4S,7S)-11-(tert-butyldimethylsilanyloxy)-3-(tert-butyldiphenylsilanyloxy)-7-hydroxy-5-(4-methoxybenzyloxy)-8,8-dimethyl-9-methyleneundecanethioic acid S-tert-butyl ester
  • CAS No.:916991-68-9
  • Molecular Formula:C48H74O6SSi2
  • Molecular Weight:835.349
  • Hs Code.:
(2R,4S,7S)-11-(tert-butyldimethylsilanyloxy)-3-(tert-butyldiphenylsilanyloxy)-7-hydroxy-5-(4-methoxybenzyloxy)-8,8-dimethyl-9-methyleneundecanethioic acid S-tert-butyl ester

Synonyms:(2R,4S,7S)-11-(tert-butyldimethylsilanyloxy)-3-(tert-butyldiphenylsilanyloxy)-7-hydroxy-5-(4-methoxybenzyloxy)-8,8-dimethyl-9-methyleneundecanethioic acid S-tert-butyl ester

Suppliers and Price of (2R,4S,7S)-11-(tert-butyldimethylsilanyloxy)-3-(tert-butyldiphenylsilanyloxy)-7-hydroxy-5-(4-methoxybenzyloxy)-8,8-dimethyl-9-methyleneundecanethioic acid S-tert-butyl ester
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Chemical Property of (2R,4S,7S)-11-(tert-butyldimethylsilanyloxy)-3-(tert-butyldiphenylsilanyloxy)-7-hydroxy-5-(4-methoxybenzyloxy)-8,8-dimethyl-9-methyleneundecanethioic acid S-tert-butyl ester
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Technology Process of (2R,4S,7S)-11-(tert-butyldimethylsilanyloxy)-3-(tert-butyldiphenylsilanyloxy)-7-hydroxy-5-(4-methoxybenzyloxy)-8,8-dimethyl-9-methyleneundecanethioic acid S-tert-butyl ester

There total 8 articles about (2R,4S,7S)-11-(tert-butyldimethylsilanyloxy)-3-(tert-butyldiphenylsilanyloxy)-7-hydroxy-5-(4-methoxybenzyloxy)-8,8-dimethyl-9-methyleneundecanethioic acid S-tert-butyl ester 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 2 steps
1: 991 mg / Pb(OAc)4 / benzene / 1 h / 20 °C
2: 86 percent / Me2AlCl / toluene / 1.5 h / -78 °C
With lead(IV) acetate; dimethylaluminum chloride; In toluene; benzene;
DOI:10.1016/j.tetlet.2006.09.094
Guidance literature:
Multi-step reaction with 4 steps
1: 92 percent / imidazole / dimethylformamide / 24 h / 20 °C
2: 4-methylmorpholine-N-oxide; OsO4 / 2-methyl-propan-2-ol; tetrahydrofuran; H2O / 14 h / 20 °C
3: 991 mg / Pb(OAc)4 / benzene / 1 h / 20 °C
4: 86 percent / Me2AlCl / toluene / 1.5 h / -78 °C
With 1H-imidazole; lead(IV) acetate; osmium(VIII) oxide; dimethylaluminum chloride; 4-methylmorpholine N-oxide; In tetrahydrofuran; water; N,N-dimethyl-formamide; toluene; tert-butyl alcohol; benzene;
DOI:10.1016/j.tetlet.2006.09.094
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