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C39H72O9Si4

Base Information
  • Chemical Name:C39H72O9Si4
  • CAS No.:1394245-90-9
  • Molecular Formula:C39H72O9Si4
  • Molecular Weight:797.337
  • Hs Code.:
C<sub>39</sub>H<sub>72</sub>O<sub>9</sub>Si<sub>4</sub>

Synonyms:C39H72O9Si4

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Chemical Property of C39H72O9Si4
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Technology Process of C39H72O9Si4

There total 11 articles about C39H72O9Si4 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 dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; at 0 ℃; for 4h; regioselective reaction;
DOI:10.1016/j.tet.2012.06.105
Guidance literature:
Multi-step reaction with 11 steps
1: methanol; sodium tetrahydroborate / 1.5 h / 20 °C
2: dmap; triethylamine / dichloromethane / 0.75 h / 20 °C
3: N-ethyl-N,N-diisopropylamine / dichloromethane / 23 h / 0 - 20 °C
4: tetrabutyl ammonium fluoride / tetrahydrofuran / 4.5 h / 20 °C
5: sodium hydride / tetrahydrofuran; mineral oil / 17 h / 0 - 20 °C
6: hydrogenchloride / water / 3 h / 0 - 50 °C
7: hydrogenchloride; water / 1,4-dioxane / 5 h / 90 °C
8: silver carbonate / toluene / 6 h / 80 °C
9: 1H-imidazole / N,N-dimethyl-formamide / 17 h / 20 °C
10: 20 % Pd(OH)2/C; hydrogen / ethanol / 1 h / 20 °C
11: dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 4 h / 0 °C
With 1H-imidazole; hydrogenchloride; methanol; dmap; sodium tetrahydroborate; 20 % Pd(OH)2/C; tetrabutyl ammonium fluoride; water; hydrogen; sodium hydride; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; N-ethyl-N,N-diisopropylamine; silver carbonate; In tetrahydrofuran; 1,4-dioxane; ethanol; dichloromethane; water; N,N-dimethyl-formamide; toluene; mineral oil; 8: Fetizon oxidation;
DOI:10.1016/j.tet.2012.06.105
Guidance literature:
Multi-step reaction with 7 steps
1: sodium hydride / tetrahydrofuran; mineral oil / 17 h / 0 - 20 °C
2: hydrogenchloride / water / 3 h / 0 - 50 °C
3: hydrogenchloride; water / 1,4-dioxane / 5 h / 90 °C
4: silver carbonate / toluene / 6 h / 80 °C
5: 1H-imidazole / N,N-dimethyl-formamide / 17 h / 20 °C
6: 20 % Pd(OH)2/C; hydrogen / ethanol / 1 h / 20 °C
7: dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 4 h / 0 °C
With 1H-imidazole; hydrogenchloride; dmap; 20 % Pd(OH)2/C; water; hydrogen; sodium hydride; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; silver carbonate; In tetrahydrofuran; 1,4-dioxane; ethanol; dichloromethane; water; N,N-dimethyl-formamide; toluene; mineral oil; 4: Fetizon oxidation;
DOI:10.1016/j.tet.2012.06.105
upstream raw materials:

C22H36O6Si

C24H40O7Si

C20H22O6

caffeic acid

Downstream raw materials:

trans-caffeoyl-6-O-D-glucono-γ-lactone

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