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C28H44O6

Base Information
  • Chemical Name:C28H44O6
  • CAS No.:1309955-95-0
  • Molecular Formula:C28H44O6
  • Molecular Weight:476.654
  • Hs Code.:
C<sub>28</sub>H<sub>44</sub>O<sub>6</sub>

Synonyms:C28H44O6

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Chemical Property of C28H44O6
Chemical Property:
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Technology Process of C28H44O6

There total 17 articles about C28H44O6 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 tetrabutyl ammonium fluoride; In tetrahydrofuran; at 130 ℃; for 1h; Inert atmosphere; Microwave irradiation;
DOI:10.1021/ol200966z
Guidance literature:
Multi-step reaction with 13 steps
1.1: sodium hydride / N,N-dimethyl-formamide / 25 - 60 °C / Inert atmosphere
1.2: 15 h / 25 °C / Inert atmosphere
2.1: borane-THF / tetrahydrofuran / 72 h / 0 °C / Inert atmosphere
2.2: 0 - 25 °C / Inert atmosphere
3.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 15 h / 20 °C / Inert atmosphere
4.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 1 h / 130 °C / Microwave irradiation; Inert atmosphere
5.1: Dess-Martin periodane / dichloromethane / 2 h / 0 °C / Inert atmosphere
6.1: sodium hydride / methanol / 0 - 25 °C / Inert atmosphere
7.1: triethylamine / dichloromethane / 4 h / 25 °C / Inert atmosphere
8.1: potassium tert-butylate / tert-butyl alcohol / 0.5 h / 25 °C / Inert atmosphere
9.1: ammonia; lithium / tetrahydrofuran; ethanol / -78 °C / Inert atmosphere
10.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 0 - 20 °C / Inert atmosphere
10.2: 0.5 h / 0 °C / Inert atmosphere
11.1: sodium tetrahydroborate / tetrahydrofuran; ethanol / 3 h / -78 °C / Inert atmosphere
12.1: sodium hydride / N,N-dimethyl-formamide / 0.5 h / 60 °C / Inert atmosphere
12.2: 15 h / 20 °C / Inert atmosphere
13.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 1 h / 130 °C / Inert atmosphere; Microwave irradiation
With sodium tetrahydroborate; borane-THF; potassium tert-butylate; tetrabutyl ammonium fluoride; ammonia; lithium; sodium hydride; Dess-Martin periodane; triethylamine; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; methanol; ethanol; dichloromethane; N,N-dimethyl-formamide; tert-butyl alcohol; 2.1: Hydroboration reaction / 7.1: Michael addition / 8.1: Robinson cyclization;
DOI:10.1021/ol200966z
Guidance literature:
Multi-step reaction with 14 steps
1.1: sodium tetrahydroborate / methanol / 0.5 h / 0 °C / Inert atmosphere
2.1: sodium hydride / N,N-dimethyl-formamide / 25 - 60 °C / Inert atmosphere
2.2: 15 h / 25 °C / Inert atmosphere
3.1: borane-THF / tetrahydrofuran / 72 h / 0 °C / Inert atmosphere
3.2: 0 - 25 °C / Inert atmosphere
4.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 15 h / 20 °C / Inert atmosphere
5.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 1 h / 130 °C / Microwave irradiation; Inert atmosphere
6.1: Dess-Martin periodane / dichloromethane / 2 h / 0 °C / Inert atmosphere
7.1: sodium hydride / methanol / 0 - 25 °C / Inert atmosphere
8.1: triethylamine / dichloromethane / 4 h / 25 °C / Inert atmosphere
9.1: potassium tert-butylate / tert-butyl alcohol / 0.5 h / 25 °C / Inert atmosphere
10.1: ammonia; lithium / tetrahydrofuran; ethanol / -78 °C / Inert atmosphere
11.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 0 - 20 °C / Inert atmosphere
11.2: 0.5 h / 0 °C / Inert atmosphere
12.1: sodium tetrahydroborate / tetrahydrofuran; ethanol / 3 h / -78 °C / Inert atmosphere
13.1: sodium hydride / N,N-dimethyl-formamide / 0.5 h / 60 °C / Inert atmosphere
13.2: 15 h / 20 °C / Inert atmosphere
14.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 1 h / 130 °C / Inert atmosphere; Microwave irradiation
With sodium tetrahydroborate; borane-THF; potassium tert-butylate; tetrabutyl ammonium fluoride; ammonia; lithium; sodium hydride; Dess-Martin periodane; triethylamine; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; methanol; ethanol; dichloromethane; N,N-dimethyl-formamide; tert-butyl alcohol; 3.1: Hydroboration reaction / 8.1: Michael addition / 9.1: Robinson cyclization;
DOI:10.1021/ol200966z
upstream raw materials:

C27H42O3Si

C27H44O3Si

C34H50O3Si

C34H52O4Si

Downstream raw materials:

C44H60O6Si

C44H60O5Si

C44H60O6Si

C28H42O6

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