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C27H50N2O5Si2

Base Information
  • Chemical Name:C27H50N2O5Si2
  • CAS No.:1567326-66-2
  • Molecular Formula:C27H50N2O5Si2
  • Molecular Weight:538.875
  • Hs Code.:
C<sub>27</sub>H<sub>50</sub>N<sub>2</sub>O<sub>5</sub>Si<sub>2</sub>

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Chemical Property of C27H50N2O5Si2
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Technology Process of C27H50N2O5Si2

There total 14 articles about C27H50N2O5Si2 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 14 steps
1.1: iodine / 16 h / 20 °C
2.1: sodium cyanide / water / 12 h / 50 °C
2.2: 12 h / 20 °C
3.1: pyridine; trifluoromethylsulfonic anhydride / dichloromethane / 0.25 h / -30 °C
3.2: 20 h / 20 °C
4.1: acetic acid / water / 3.5 h / 50 °C
5.1: triethylamine; dmap / dichloromethane / 12 h / 20 °C
6.1: Dess-Martin periodane / dichloromethane / 3 h / 0 - 20 °C
7.1: triethyl phosphite / tetrahydrofuran / 16 h / 20 °C / Inert atmosphere
8.1: acetic acid; sodium cyanoborohydride / 0.5 h / 20 °C
9.1: tetrahydrofuran; methanol / 2 h / 20 °C
10.1: potassium carbonate / N,N-dimethyl-formamide
11.1: acetic acid; methanol
12.1: toluene-4-sulfonic acid; trimethyl orthoformate / methanol / 75 °C
13.1: dichloromethane
14.1: toluene-4-sulfonic acid; methanol
With pyridine; methanol; dmap; sodium cyanide; trifluoromethylsulfonic anhydride; iodine; sodium cyanoborohydride; potassium carbonate; Dess-Martin periodane; toluene-4-sulfonic acid; acetic acid; triethylamine; triethyl phosphite; trimethyl orthoformate; In tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide;
Guidance literature:
Multi-step reaction with 13 steps
1.1: sodium cyanide / water / 12 h / 50 °C
1.2: 12 h / 20 °C
2.1: pyridine; trifluoromethylsulfonic anhydride / dichloromethane / 0.25 h / -30 °C
2.2: 20 h / 20 °C
3.1: acetic acid / water / 3.5 h / 50 °C
4.1: triethylamine; dmap / dichloromethane / 12 h / 20 °C
5.1: Dess-Martin periodane / dichloromethane / 3 h / 0 - 20 °C
6.1: triethyl phosphite / tetrahydrofuran / 16 h / 20 °C / Inert atmosphere
7.1: acetic acid; sodium cyanoborohydride / 0.5 h / 20 °C
8.1: tetrahydrofuran; methanol / 2 h / 20 °C
9.1: potassium carbonate / N,N-dimethyl-formamide
10.1: acetic acid; methanol
11.1: toluene-4-sulfonic acid; trimethyl orthoformate / methanol / 75 °C
12.1: dichloromethane
13.1: toluene-4-sulfonic acid; methanol
With pyridine; methanol; dmap; sodium cyanide; trifluoromethylsulfonic anhydride; sodium cyanoborohydride; potassium carbonate; Dess-Martin periodane; toluene-4-sulfonic acid; acetic acid; triethylamine; triethyl phosphite; trimethyl orthoformate; In tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide;
Guidance literature:
Multi-step reaction with 12 steps
1.1: pyridine; trifluoromethylsulfonic anhydride / dichloromethane / 0.25 h / -30 °C
1.2: 20 h / 20 °C
2.1: acetic acid / water / 3.5 h / 50 °C
3.1: triethylamine; dmap / dichloromethane / 12 h / 20 °C
4.1: Dess-Martin periodane / dichloromethane / 3 h / 0 - 20 °C
5.1: triethyl phosphite / tetrahydrofuran / 16 h / 20 °C / Inert atmosphere
6.1: acetic acid; sodium cyanoborohydride / 0.5 h / 20 °C
7.1: tetrahydrofuran; methanol / 2 h / 20 °C
8.1: potassium carbonate / N,N-dimethyl-formamide
9.1: acetic acid; methanol
10.1: toluene-4-sulfonic acid; trimethyl orthoformate / methanol / 75 °C
11.1: dichloromethane
12.1: toluene-4-sulfonic acid; methanol
With pyridine; methanol; dmap; trifluoromethylsulfonic anhydride; sodium cyanoborohydride; potassium carbonate; Dess-Martin periodane; toluene-4-sulfonic acid; acetic acid; triethylamine; triethyl phosphite; trimethyl orthoformate; In tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide;
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