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C47H47BrCl4N8O10Si

Base Information
  • Chemical Name:C47H47BrCl4N8O10Si
  • CAS No.:1370458-17-5
  • Molecular Formula:C47H47BrCl4N8O10Si
  • Molecular Weight:1133.74
  • Hs Code.:
C<sub>47</sub>H<sub>47</sub>BrCl<sub>4</sub>N<sub>8</sub>O<sub>10</sub>Si

Synonyms:C47H47BrCl4N8O10Si

Suppliers and Price of C47H47BrCl4N8O10Si
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Chemical Property of C47H47BrCl4N8O10Si
Chemical Property:
Purity/Quality:

98% *data from raw suppliers

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Technology Process of C47H47BrCl4N8O10Si

There total 20 articles about C47H47BrCl4N8O10Si 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:
C56H65BrCl4N8O13Si; With triethylsilane; trifluoroacetic acid; In dichloromethane; at 20 ℃; for 4h; Cooling with ice; Inert atmosphere;
With N-ethyl-N,N-diisopropylamine; ((3H-[1,2,3]triazolo[4,5-b]pyridin-3-yl)oxy)tri(pyrrolidin-1-yl)phosphonium hexafluorophosphate(V); In dichloromethane; N,N-dimethyl-formamide; at 20 ℃; Inert atmosphere; Cooling with ice;
DOI:10.1021/ol300576n
Guidance literature:
Multi-step reaction with 5 steps
1.1: thionyl chloride; N,N-dimethyl-formamide / dichloromethane / Inert atmosphere
2.1: toluene / 6.5 h / 20 - 80 °C / Inert atmosphere
3.1: diisopropylamine / acetonitrile / 20 °C / Inert atmosphere
4.1: 1-hydroxy-7-aza-benzotriazole; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 1 h / 0 °C / Cooling with ice; Inert atmosphere
4.2: 0 - 20 °C / Inert atmosphere
5.1: triethylsilane; trifluoroacetic acid / dichloromethane / 4 h / 20 °C / Cooling with ice; Inert atmosphere
5.2: 20 °C / Inert atmosphere; Cooling with ice
With triethylsilane; thionyl chloride; 1-hydroxy-7-aza-benzotriazole; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; diisopropylamine; N,N-dimethyl-formamide; trifluoroacetic acid; In dichloromethane; N,N-dimethyl-formamide; toluene; acetonitrile;
DOI:10.1021/ol300576n
Guidance literature:
Multi-step reaction with 6 steps
1.1: sodium hydroxide / tetrahydrofuran; methanol; water / 20 °C / Cooling with ice; Inert atmosphere
2.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 1 h / 0 °C / Inert atmosphere
3.1: dichloromethane / 0 - 20 °C / Inert atmosphere
4.1: lithium hydroxide / tetrahydrofuran; water / 3 h / 20 °C / Cooling with ice
5.1: 1-hydroxy-7-aza-benzotriazole; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 1 h / 0 °C / Cooling with ice; Inert atmosphere
5.2: 0 - 20 °C / Inert atmosphere
6.1: triethylsilane; trifluoroacetic acid / dichloromethane / 4 h / 20 °C / Cooling with ice; Inert atmosphere
6.2: 20 °C / Inert atmosphere; Cooling with ice
With triethylsilane; 1-hydroxy-7-aza-benzotriazole; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; trifluoroacetic acid; sodium hydroxide; lithium hydroxide; In tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide;
DOI:10.1021/ol300576n
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