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C50H84O7Si2

Base Information
  • Chemical Name:C50H84O7Si2
  • CAS No.:1234064-59-5
  • Molecular Formula:C50H84O7Si2
  • Molecular Weight:853.384
  • Hs Code.:
C<sub>50</sub>H<sub>84</sub>O<sub>7</sub>Si<sub>2</sub>

Synonyms:C50H84O7Si2

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Chemical Property of C50H84O7Si2
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Technology Process of C50H84O7Si2

There total 31 articles about C50H84O7Si2 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 pyridine; pyridine hydrofluoride; In tetrahydrofuran; for 0.75h;
DOI:10.1016/j.tet.2011.07.066
Guidance literature:
Multi-step reaction with 9 steps
1.1: 2,6-dimethylpyridine / dichloromethane / 1.5 h / -78 - 20 °C
2.1: pyridinium p-toluenesulfonate / methanol; dichloromethane / 0.25 h
3.1: sodium hydrogencarbonate; Dess-Martin periodane / dichloromethane / 1 h
4.1: tin(IV) chloride / dichloromethane / 0.75 h / -78 °C
4.2: 3 h / -78 °C
4.3: -78 - 20 °C
5.1: 2,6-dimethylpyridine / dichloromethane / 1.5 h / 0 - 20 °C
6.1: pyridine; pyridine hydrofluoride / tetrahydrofuran / 0.5 h
7.1: scandium tris(trifluoromethanesulfonate) / toluene / 3 h
8.1: tert.-butyl lithium; 9-methoxy-9-BBN / tetrahydrofuran; diethyl ether; hexane; pentane / 1.08 h / -78 - 20 °C
8.2: 20 °C
9.1: pyridine; pyridine hydrofluoride / tetrahydrofuran / 0.75 h
With pyridine; 2,6-dimethylpyridine; pyridine hydrofluoride; tert.-butyl lithium; pyridinium p-toluenesulfonate; tin(IV) chloride; sodium hydrogencarbonate; Dess-Martin periodane; 9-methoxy-9-BBN; scandium tris(trifluoromethanesulfonate); In tetrahydrofuran; methanol; diethyl ether; hexane; dichloromethane; toluene; pentane; 4.1: Sakurai reaction / 4.2: Sakurai reaction / 8.2: Suzuki-Miyaura coupling;
DOI:10.1016/j.tet.2011.07.066
Guidance literature:
Multi-step reaction with 10 steps
1.1: pyridinium p-toluenesulfonate; toluene-4-sulfonic acid / methanol / 2 h
2.1: 2,6-dimethylpyridine / dichloromethane / 1.5 h / -78 - 20 °C
3.1: pyridinium p-toluenesulfonate / methanol; dichloromethane / 0.25 h
4.1: sodium hydrogencarbonate; Dess-Martin periodane / dichloromethane / 1 h
5.1: tin(IV) chloride / dichloromethane / 0.75 h / -78 °C
5.2: 3 h / -78 °C
5.3: -78 - 20 °C
6.1: 2,6-dimethylpyridine / dichloromethane / 1.5 h / 0 - 20 °C
7.1: pyridine; pyridine hydrofluoride / tetrahydrofuran / 0.5 h
8.1: scandium tris(trifluoromethanesulfonate) / toluene / 3 h
9.1: tert.-butyl lithium; 9-methoxy-9-BBN / tetrahydrofuran; diethyl ether; hexane; pentane / 1.08 h / -78 - 20 °C
9.2: 20 °C
10.1: pyridine; pyridine hydrofluoride / tetrahydrofuran / 0.75 h
With pyridine; 2,6-dimethylpyridine; pyridine hydrofluoride; tert.-butyl lithium; pyridinium p-toluenesulfonate; tin(IV) chloride; sodium hydrogencarbonate; Dess-Martin periodane; toluene-4-sulfonic acid; 9-methoxy-9-BBN; scandium tris(trifluoromethanesulfonate); In tetrahydrofuran; methanol; diethyl ether; hexane; dichloromethane; toluene; pentane; 5.1: Sakurai reaction / 5.2: Sakurai reaction / 9.2: Suzuki-Miyaura coupling;
DOI:10.1016/j.tet.2011.07.066
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