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C52H90O12SSi2

Base Information
  • Chemical Name:C52H90O12SSi2
  • CAS No.:1316279-00-1
  • Molecular Formula:C52H90O12SSi2
  • Molecular Weight:995.516
  • Hs Code.:
C<sub>52</sub>H<sub>90</sub>O<sub>12</sub>SSi<sub>2</sub>

Synonyms:C52H90O12SSi2

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Chemical Property of C52H90O12SSi2
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Technology Process of C52H90O12SSi2

There total 26 articles about C52H90O12SSi2 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 acetic acid; zinc; In tetrahydrofuran; water; at 0 - 20 ℃; for 3h;
Guidance literature:
Multi-step reaction with 14 steps
1.1: 1H-imidazole / N,N-dimethyl-formamide / 2 h / 0 - 20 °C
2.1: lithium borohydride / tetrahydrofuran / 16 h / 0 - 23 °C
2.2: 0.5 h / 0 - 10 °C
3.1: dmap; triethylamine / dichloromethane / 2 h / 0 - 22 °C
4.1: zinc / methanesulfonic acid / tetrahydrofuran / 5 h / Reflux
5.1: water; acetic acid / tetrahydrofuran / 10 h / 10 - 20 °C
6.1: hydrogen / palladium 10% on activated carbon / ethyl acetate / 2 h / 20 °C
7.1: toluene / 0.25 h / 95 °C
8.1: potassium hexamethylsilazane / toluene; tetrahydrofuran / 1 h / -30 - -25 °C
9.1: hydrogenchloride / isopropyl alcohol; methanol / 1 h / 20 °C
10.1: pyridine / dichloromethane / 1 h / -10 - 0 °C
11.1: sodium iodide / dichloromethane; N,N-dimethyl-formamide / 3 h / 20 - 22 °C
12.1: triethylamine; nickel dichloride; chromium dichloride; (S)-N-(2-(4-isopropyl-4,5-dihydrooxazol-2-yl)-6-methylphenyl)methane sulfonamide / tetrahydrofuran / 20.5 h / 22 - 24 °C / Inert atmosphere
12.2: 1 h / 0 - 5 °C
13.1: dmap; pyridine / 3 h / 20 - 23 °C
14.1: zinc; acetic acid / water; tetrahydrofuran / 3 h / 0 - 20 °C
With pyridine; 1H-imidazole; chromium dichloride; hydrogenchloride; dmap; lithium borohydride; water; hydrogen; potassium hexamethylsilazane; acetic acid; triethylamine; sodium iodide; nickel dichloride; zinc; (S)-N-(2-(4-isopropyl-4,5-dihydrooxazol-2-yl)-6-methylphenyl)methane sulfonamide; methanesulfonic acid; palladium 10% on activated carbon; In tetrahydrofuran; methanol; dichloromethane; water; ethyl acetate; N,N-dimethyl-formamide; isopropyl alcohol; toluene; 12.1: Nozaki-Hiyama-Kishi Coupling / 14.1: Vasella Fragmentation;
Guidance literature:
Multi-step reaction with 11 steps
1.1: zinc / methanesulfonic acid / tetrahydrofuran / 5 h / Reflux
2.1: water; acetic acid / tetrahydrofuran / 10 h / 10 - 20 °C
3.1: hydrogen / palladium 10% on activated carbon / ethyl acetate / 2 h / 20 °C
4.1: toluene / 0.25 h / 95 °C
5.1: potassium hexamethylsilazane / toluene; tetrahydrofuran / 1 h / -30 - -25 °C
6.1: hydrogenchloride / isopropyl alcohol; methanol / 1 h / 20 °C
7.1: pyridine / dichloromethane / 1 h / -10 - 0 °C
8.1: sodium iodide / dichloromethane; N,N-dimethyl-formamide / 3 h / 20 - 22 °C
9.1: triethylamine; nickel dichloride; chromium dichloride; (S)-N-(2-(4-isopropyl-4,5-dihydrooxazol-2-yl)-6-methylphenyl)methane sulfonamide / tetrahydrofuran / 20.5 h / 22 - 24 °C / Inert atmosphere
9.2: 1 h / 0 - 5 °C
10.1: dmap; pyridine / 3 h / 20 - 23 °C
11.1: zinc; acetic acid / water; tetrahydrofuran / 3 h / 0 - 20 °C
With pyridine; chromium dichloride; hydrogenchloride; dmap; water; hydrogen; potassium hexamethylsilazane; acetic acid; triethylamine; sodium iodide; nickel dichloride; zinc; (S)-N-(2-(4-isopropyl-4,5-dihydrooxazol-2-yl)-6-methylphenyl)methane sulfonamide; methanesulfonic acid; palladium 10% on activated carbon; In tetrahydrofuran; methanol; dichloromethane; water; ethyl acetate; N,N-dimethyl-formamide; isopropyl alcohol; toluene; 9.1: Nozaki-Hiyama-Kishi Coupling / 11.1: Vasella Fragmentation;
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