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C41H47NO8

Base Information
  • Chemical Name:C41H47NO8
  • CAS No.:1379450-04-0
  • Molecular Formula:C41H47NO8
  • Molecular Weight:681.826
  • Hs Code.:
C<sub>41</sub>H<sub>47</sub>NO<sub>8</sub>

Synonyms:C41H47NO8

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Chemical Property of C41H47NO8
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Technology Process of C41H47NO8

There total 10 articles about C41H47NO8 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 hydrogenfluoride; In tetrahydrofuran; at 0 - 25 ℃; Inert atmosphere;
DOI:10.1021/ja301326k
Guidance literature:
Multi-step reaction with 7 steps
1: tetrahydrofuran / -78 - 0 °C / Inert atmosphere
2: tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride / dichloromethane / 12 h / 25 °C
3: tetrahydrofuran / 0 - 25 °C / Inert atmosphere; Molecular sieve
4: pyridinium chlorochromate / dichloromethane / 4 h / 25 °C / Inert atmosphere; Molecular sieve
5: 2,6-di-tert-butyl-pyridine / nitromethane / 2 h / -20 °C / Inert atmosphere; Molecular sieve
6: copper(l) iodide; tetrakis(triphenylphosphine) palladium(0); Tetrabutylammoniumsalz der Diphenylphosphinsaeure / N,N-dimethyl-formamide / 16 h / 45 °C / Inert atmosphere
7: pyridine; pyridine hydrogenfluoride / tetrahydrofuran / 0 - 25 °C / Inert atmosphere
With pyridine; tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride; copper(l) iodide; tetrakis(triphenylphosphine) palladium(0); 2,6-di-tert-butyl-pyridine; pyridine hydrogenfluoride; Tetrabutylammoniumsalz der Diphenylphosphinsaeure; pyridinium chlorochromate; In tetrahydrofuran; nitromethane; dichloromethane; N,N-dimethyl-formamide; 5: Friedel Crafts acylation / 6: Stille coupling;
DOI:10.1021/ja301326k
Guidance literature:
Multi-step reaction with 8 steps
1.1: sodium hydride / N,N-dimethyl-formamide / 1 h / 0 °C
1.2: 6 h / 0 °C
2.1: tetrahydrofuran / -78 - 0 °C / Inert atmosphere
3.1: tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride / dichloromethane / 12 h / 25 °C
4.1: tetrahydrofuran / 0 - 25 °C / Inert atmosphere; Molecular sieve
5.1: pyridinium chlorochromate / dichloromethane / 4 h / 25 °C / Inert atmosphere; Molecular sieve
6.1: 2,6-di-tert-butyl-pyridine / nitromethane / 2 h / -20 °C / Inert atmosphere; Molecular sieve
7.1: copper(l) iodide; tetrakis(triphenylphosphine) palladium(0); Tetrabutylammoniumsalz der Diphenylphosphinsaeure / N,N-dimethyl-formamide / 16 h / 45 °C / Inert atmosphere
8.1: pyridine; pyridine hydrogenfluoride / tetrahydrofuran / 0 - 25 °C / Inert atmosphere
With pyridine; tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride; copper(l) iodide; tetrakis(triphenylphosphine) palladium(0); 2,6-di-tert-butyl-pyridine; sodium hydride; pyridine hydrogenfluoride; Tetrabutylammoniumsalz der Diphenylphosphinsaeure; pyridinium chlorochromate; In tetrahydrofuran; nitromethane; dichloromethane; N,N-dimethyl-formamide; 6.1: Friedel Crafts acylation / 7.1: Stille coupling;
DOI:10.1021/ja301326k
upstream raw materials:

C18H28N2O6

C21H32N2O6

C21H29NO5

C19H25NO5

Downstream raw materials:

C41H46INO7

C42H49NO10S

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