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ethyl (E,E,E,E)-16-benzyloxy-2,6,10,14-tetramethyl-2,6,10,14-hexadecatetraenoate

Base Information
  • Chemical Name:ethyl (E,E,E,E)-16-benzyloxy-2,6,10,14-tetramethyl-2,6,10,14-hexadecatetraenoate
  • CAS No.:857463-56-0
  • Molecular Formula:C29H42O3
  • Molecular Weight:438.651
  • Hs Code.:
ethyl (E,E,E,E)-16-benzyloxy-2,6,10,14-tetramethyl-2,6,10,14-hexadecatetraenoate

Synonyms:ethyl (E,E,E,E)-16-benzyloxy-2,6,10,14-tetramethyl-2,6,10,14-hexadecatetraenoate

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Chemical Property of ethyl (E,E,E,E)-16-benzyloxy-2,6,10,14-tetramethyl-2,6,10,14-hexadecatetraenoate
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Technology Process of ethyl (E,E,E,E)-16-benzyloxy-2,6,10,14-tetramethyl-2,6,10,14-hexadecatetraenoate

There total 5 articles about ethyl (E,E,E,E)-16-benzyloxy-2,6,10,14-tetramethyl-2,6,10,14-hexadecatetraenoate 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:
Multi-step reaction with 3 steps
1: 82 percent / HClO4 / tetrahydrofuran; H2O / 0.83 h / 20 °C
2: 96 percent / NaIO4 / tetrahydrofuran; H2O / 17 h / 20 °C
3: 98 percent / CH2Cl2 / 0 - 20 °C
With sodium periodate; perchloric acid; In tetrahydrofuran; dichloromethane; water; 3: Wittig reaction;
DOI:10.1021/jo0502091
Guidance literature:
Multi-step reaction with 2 steps
1: 96 percent / NaIO4 / tetrahydrofuran; H2O / 17 h / 20 °C
2: 98 percent / CH2Cl2 / 0 - 20 °C
With sodium periodate; In tetrahydrofuran; dichloromethane; water; 2: Wittig reaction;
DOI:10.1021/jo0502091
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