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[4-methyl-2,6-bis-(5-methyl-2-pentafluorophenyloxycarbonylmethoxy-benzyl)-phenoxy]-acetic acid pentafluorophenyl ester

Base Information Edit
  • Chemical Name:[4-methyl-2,6-bis-(5-methyl-2-pentafluorophenyloxycarbonylmethoxy-benzyl)-phenoxy]-acetic acid pentafluorophenyl ester
  • CAS No.:518361-66-5
  • Molecular Formula:C47H27F15O9
  • Molecular Weight:1020.7
  • Hs Code.:
  • Mol file:518361-66-5.mol
[4-methyl-2,6-bis-(5-methyl-2-pentafluorophenyloxycarbonylmethoxy-benzyl)-phenoxy]-acetic acid pentafluorophenyl ester

Synonyms:[4-methyl-2,6-bis-(5-methyl-2-pentafluorophenyloxycarbonylmethoxy-benzyl)-phenoxy]-acetic acid pentafluorophenyl ester

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Chemical Property of [4-methyl-2,6-bis-(5-methyl-2-pentafluorophenyloxycarbonylmethoxy-benzyl)-phenoxy]-acetic acid pentafluorophenyl ester Edit
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Technology Process of [4-methyl-2,6-bis-(5-methyl-2-pentafluorophenyloxycarbonylmethoxy-benzyl)-phenoxy]-acetic acid pentafluorophenyl ester

There total 3 articles about [4-methyl-2,6-bis-(5-methyl-2-pentafluorophenyloxycarbonylmethoxy-benzyl)-phenoxy]-acetic acid pentafluorophenyl ester 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: 36 percent / sodium hydride / dimethylformamide / 2 h / 80 °C
2: 73 percent / tetramethylammonium hydroxide / tetrahydrofuran; H2O / 24 h / Heating
3: 86 percent / N,N-dicyclohexylcarbodiimide / dimethylformamide; ethyl acetate / 1 h / 0 °C
With tetramethyl ammoniumhydroxide; sodium hydride; dicyclohexyl-carbodiimide; In tetrahydrofuran; water; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1081/SCC-120015403
Guidance literature:
Multi-step reaction with 2 steps
1: 73 percent / tetramethylammonium hydroxide / tetrahydrofuran; H2O / 24 h / Heating
2: 86 percent / N,N-dicyclohexylcarbodiimide / dimethylformamide; ethyl acetate / 1 h / 0 °C
With tetramethyl ammoniumhydroxide; dicyclohexyl-carbodiimide; In tetrahydrofuran; water; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1081/SCC-120015403
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