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C36H37NO5

Base Information
  • Chemical Name:C36H37NO5
  • CAS No.:1379450-00-6
  • Molecular Formula:C36H37NO5
  • Molecular Weight:563.693
  • Hs Code.:
C<sub>36</sub>H<sub>37</sub>NO<sub>5</sub>

Synonyms:C36H37NO5

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Chemical Property of C36H37NO5
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Technology Process of C36H37NO5

There total 9 articles about C36H37NO5 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 ammonium fluoride; In methanol; at 25 ℃; for 1h; Inert atmosphere;
DOI:10.1021/ja301326k
Guidance literature:
Multi-step reaction with 10 steps
1.1: tetrahydrofuran / -78 - 0 °C / Inert atmosphere
2.1: tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride / dichloromethane / 12 h / 25 °C
3.1: tetrahydrofuran / 0 - 25 °C / Inert atmosphere; Molecular sieve
4.1: pyridinium chlorochromate / dichloromethane / 4 h / 25 °C / Inert atmosphere; Molecular sieve
5.1: 2,6-di-tert-butyl-pyridine / nitromethane / 2 h / -20 °C / Inert atmosphere; Molecular sieve
6.1: copper(l) iodide; tetrakis(triphenylphosphine) palladium(0); cesium fluoride / N,N-dimethyl-formamide / 16 h / 45 °C / Inert atmosphere
7.1: trifluoroacetic acid / dichloromethane / 0 - 25 °C / Inert atmosphere
8.1: 1,1'-carbonyldiimidazole / N,N-dimethyl-formamide / 2 h / 25 °C / Inert atmosphere
8.2: 16 h / 20 °C / Inert atmosphere
9.1: lithium aluminium tetrahydride; aluminum (III) chloride / tetrahydrofuran / 0 - 25 °C / Inert atmosphere
10.1: ammonium fluoride / methanol / 1 h / 25 °C / Inert atmosphere
With tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride; aluminum (III) chloride; ammonium fluoride; copper(l) iodide; lithium aluminium tetrahydride; tetrakis(triphenylphosphine) palladium(0); 2,6-di-tert-butyl-pyridine; cesium fluoride; 1,1'-carbonyldiimidazole; pyridinium chlorochromate; trifluoroacetic acid; In tetrahydrofuran; methanol; nitromethane; dichloromethane; N,N-dimethyl-formamide; 5.1: Friedel Crafts acylation / 6.1: Stille coupling;
DOI:10.1021/ja301326k
Guidance literature:
Multi-step reaction with 11 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); cesium fluoride / N,N-dimethyl-formamide / 16 h / 45 °C / Inert atmosphere
8.1: trifluoroacetic acid / dichloromethane / 0 - 25 °C / Inert atmosphere
9.1: 1,1'-carbonyldiimidazole / N,N-dimethyl-formamide / 2 h / 25 °C / Inert atmosphere
9.2: 16 h / 20 °C / Inert atmosphere
10.1: lithium aluminium tetrahydride; aluminum (III) chloride / tetrahydrofuran / 0 - 25 °C / Inert atmosphere
11.1: ammonium fluoride / methanol / 1 h / 25 °C / Inert atmosphere
With tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride; aluminum (III) chloride; ammonium fluoride; copper(l) iodide; lithium aluminium tetrahydride; tetrakis(triphenylphosphine) palladium(0); 2,6-di-tert-butyl-pyridine; sodium hydride; cesium fluoride; 1,1'-carbonyldiimidazole; pyridinium chlorochromate; trifluoroacetic acid; In tetrahydrofuran; methanol; nitromethane; dichloromethane; N,N-dimethyl-formamide; 6.1: Friedel Crafts acylation / 7.1: Stille coupling;
DOI:10.1021/ja301326k
upstream raw materials:

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