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(8R,9R,10S)-9-Benzyloxy-11-(tert-butyl-diphenyl-silanyloxy)-4,6,8,10-tetramethyl-undecane-3,5,7-trione

Base Information Edit
  • Chemical Name:(8R,9R,10S)-9-Benzyloxy-11-(tert-butyl-diphenyl-silanyloxy)-4,6,8,10-tetramethyl-undecane-3,5,7-trione
  • CAS No.:160488-44-8
  • Molecular Formula:C38H50O5Si
  • Molecular Weight:614.897
  • Hs Code.:
  • Mol file:160488-44-8.mol
(8R,9R,10S)-9-Benzyloxy-11-(tert-butyl-diphenyl-silanyloxy)-4,6,8,10-tetramethyl-undecane-3,5,7-trione

Synonyms:

Suppliers and Price of (8R,9R,10S)-9-Benzyloxy-11-(tert-butyl-diphenyl-silanyloxy)-4,6,8,10-tetramethyl-undecane-3,5,7-trione
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of (8R,9R,10S)-9-Benzyloxy-11-(tert-butyl-diphenyl-silanyloxy)-4,6,8,10-tetramethyl-undecane-3,5,7-trione Edit
Chemical Property:
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Technology Process of (8R,9R,10S)-9-Benzyloxy-11-(tert-butyl-diphenyl-silanyloxy)-4,6,8,10-tetramethyl-undecane-3,5,7-trione

There total 9 articles about (8R,9R,10S)-9-Benzyloxy-11-(tert-butyl-diphenyl-silanyloxy)-4,6,8,10-tetramethyl-undecane-3,5,7-trione 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 9 steps
1: p-TsOH / CH2Cl2
2: DIBAL-H / CH2Cl2 / 0 °C
3: 100 percent / pyridine
4: 1.) O3, 2.) Me2S / 1.) CH2Cl2, MeOH
5: NaBH4
6: imidazole
7: 99 percent / K2CO3 / methanol
8: 2.) KMnO4 / 1.) Swern oxid.
9: 1.) (COCl)2, 2.) LDA / 2.) DMPU, -70 deg C
With pyridine; 1H-imidazole; sodium tetrahydroborate; potassium permanganate; oxalyl dichloride; dimethylsulfide; diisobutylaluminium hydride; potassium carbonate; toluene-4-sulfonic acid; ozone; lithium diisopropyl amide; In methanol; dichloromethane;
DOI:10.1016/0040-4039(94)88516-8
Guidance literature:
Multi-step reaction with 7 steps
1: 100 percent / pyridine
2: 1.) O3, 2.) Me2S / 1.) CH2Cl2, MeOH
3: NaBH4
4: imidazole
5: 99 percent / K2CO3 / methanol
6: 2.) KMnO4 / 1.) Swern oxid.
7: 1.) (COCl)2, 2.) LDA / 2.) DMPU, -70 deg C
With pyridine; 1H-imidazole; sodium tetrahydroborate; potassium permanganate; oxalyl dichloride; dimethylsulfide; potassium carbonate; ozone; lithium diisopropyl amide; In methanol;
DOI:10.1016/0040-4039(94)88516-8
Guidance literature:
Multi-step reaction with 8 steps
1: DIBAL-H / CH2Cl2 / 0 °C
2: 100 percent / pyridine
3: 1.) O3, 2.) Me2S / 1.) CH2Cl2, MeOH
4: NaBH4
5: imidazole
6: 99 percent / K2CO3 / methanol
7: 2.) KMnO4 / 1.) Swern oxid.
8: 1.) (COCl)2, 2.) LDA / 2.) DMPU, -70 deg C
With pyridine; 1H-imidazole; sodium tetrahydroborate; potassium permanganate; oxalyl dichloride; dimethylsulfide; diisobutylaluminium hydride; potassium carbonate; ozone; lithium diisopropyl amide; In methanol; dichloromethane;
DOI:10.1016/0040-4039(94)88516-8
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