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C36H58N4O7SSi

Base Information Edit
  • Chemical Name:C36H58N4O7SSi
  • CAS No.:1300655-99-5
  • Molecular Formula:C36H58N4O7SSi
  • Molecular Weight:719.031
  • Hs Code.:
  • Mol file:1300655-99-5.mol
C<sub>36</sub>H<sub>58</sub>N<sub>4</sub>O<sub>7</sub>SSi

Synonyms:C36H58N4O7SSi

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Chemical Property of C36H58N4O7SSi Edit
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Technology Process of C36H58N4O7SSi

There total 18 articles about C36H58N4O7SSi 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 di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran; for 24h; Inert atmosphere;
DOI:10.1021/ja201467z
Guidance literature:
Multi-step reaction with 15 steps
1.1: n-butyllithium / hexane; tert-butyl methyl ether / 0.17 h / -78 °C / Inert atmosphere
1.2: 0.67 h / 0 - 20 °C / Inert atmosphere
2.1: sodium hydride / hexane / 2 h / Inert atmosphere; Reflux
3.1: acetylacetonatodicarbonylrhodium(l) / benzene / 4.5 h / 60 °C / 51716.2 Torr / Autoclave
3.2: 1 h / 40 °C / Inert atmosphere
4.1: 2,6-dimethylpyridine / dichloromethane / 1 h / -78 °C / Inert atmosphere
5.1: diisobutylaluminium hydride / tetrahydrofuran; hexane / -78 °C / Inert atmosphere
5.2: -78 - 20 °C / Inert atmosphere
6.1: toluene / 18 h / Inert atmosphere; Reflux
7.1: osmium(VIII) oxide; water; 4-methylmorpholine N-oxide; citric acid / tetrahydrofuran; tert-butyl alcohol / 24 h / Inert atmosphere
8.1: sodium periodate; sodium hydrogencarbonate / tetrahydrofuran; water / 1 h / 0 °C / Inert atmosphere
9.1: tetra-(n-butyl)ammonium iodide / dichloromethane; water / 3 h / Inert atmosphere
10.1: acetylacetonatodicarbonylrhodium(l); hydrogen; triphenylphosphine / tetrahydrofuran / 24 h / 20 - 50 °C / 25858.1 Torr / Autoclave
11.1: pyridine; dmap / dichloromethane / 16 h / -20 °C / Inert atmosphere
12.1: titanium tetrachloride / dichloromethane / 0.08 h / 0 °C / Inert atmosphere
12.2: 3 h / -40 °C / Inert atmosphere
13.1: dmap / 24 h / Inert atmosphere
14.1: 5% Pd(II)/C(eggshell); hydrogen / tetrahydrofuran / 2 h / 760.05 Torr
15.1: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / 24 h / Inert atmosphere
With pyridine; 2,6-dimethylpyridine; dmap; acetylacetonatodicarbonylrhodium(l); sodium periodate; osmium(VIII) oxide; n-butyllithium; di-isopropyl azodicarboxylate; 5% Pd(II)/C(eggshell); water; hydrogen; titanium tetrachloride; tetra-(n-butyl)ammonium iodide; sodium hydride; diisobutylaluminium hydride; sodium hydrogencarbonate; 4-methylmorpholine N-oxide; triphenylphosphine; citric acid; In tetrahydrofuran; hexane; dichloromethane; tert-butyl methyl ether; water; toluene; tert-butyl alcohol; benzene; 9.1: Felkin addition;
DOI:10.1021/ja201467z
Guidance literature:
Multi-step reaction with 5 steps
1.1: pyridine; dmap / dichloromethane / 16 h / -20 °C / Inert atmosphere
2.1: titanium tetrachloride / dichloromethane / 0.08 h / 0 °C / Inert atmosphere
2.2: 3 h / -40 °C / Inert atmosphere
3.1: dmap / 24 h / Inert atmosphere
4.1: 5% Pd(II)/C(eggshell); hydrogen / tetrahydrofuran / 2 h / 760.05 Torr
5.1: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / 24 h / Inert atmosphere
With pyridine; dmap; di-isopropyl azodicarboxylate; 5% Pd(II)/C(eggshell); hydrogen; titanium tetrachloride; triphenylphosphine; In tetrahydrofuran; dichloromethane;
DOI:10.1021/ja201467z
upstream raw materials:

C13H18O2

C31H52O6Si

C34H56O8Si

C41H67NO7S2Si

Downstream raw materials:

C36H58N4O9SSi

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