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Methoxy-acetic acid 10-[1-(2-hydroxymethyl-phenyl)-meth-(E)-ylidene]-cyclodeca-2,8-diynyl ester

Base Information
  • Chemical Name:Methoxy-acetic acid 10-[1-(2-hydroxymethyl-phenyl)-meth-(E)-ylidene]-cyclodeca-2,8-diynyl ester
  • CAS No.:357172-89-5
  • Molecular Formula:C21H22O4
  • Molecular Weight:338.403
  • Hs Code.:
Methoxy-acetic acid 10-[1-(2-hydroxymethyl-phenyl)-meth-(E)-ylidene]-cyclodeca-2,8-diynyl ester

Synonyms:Methoxy-acetic acid 10-[1-(2-hydroxymethyl-phenyl)-meth-(E)-ylidene]-cyclodeca-2,8-diynyl ester

Suppliers and Price of Methoxy-acetic acid 10-[1-(2-hydroxymethyl-phenyl)-meth-(E)-ylidene]-cyclodeca-2,8-diynyl ester
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of Methoxy-acetic acid 10-[1-(2-hydroxymethyl-phenyl)-meth-(E)-ylidene]-cyclodeca-2,8-diynyl ester
Chemical Property:
Purity/Quality:

98% *data from raw suppliers

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Technology Process of Methoxy-acetic acid 10-[1-(2-hydroxymethyl-phenyl)-meth-(E)-ylidene]-cyclodeca-2,8-diynyl ester

There total 6 articles about Methoxy-acetic acid 10-[1-(2-hydroxymethyl-phenyl)-meth-(E)-ylidene]-cyclodeca-2,8-diynyl 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 5 steps
1: 85 percent / I2; morpholine / toluene / 18 h / 60 °C
2: 88 percent / PCC; 4 Angstroem MS / CH2Cl2 / 20 h / 20 °C
3: 25 percent / CrCl2; NiCl2 / tetrahydrofuran / 8 h / 20 °C
4: 71 percent / DCC; DMAP / CH2Cl2 / 12 h / 20 °C
5: 46 percent / PPTS / methanol / 16 h / 20 °C
With morpholine; chromium dichloride; dmap; 4 Angstroem MS; iodine; pyridinium p-toluenesulfonate; dicyclohexyl-carbodiimide; pyridinium chlorochromate; nickel dichloride; In tetrahydrofuran; methanol; dichloromethane; toluene; 3: Nozaki-Hiyama-Kishi reaction;
DOI:10.1016/S0040-4039(01)00708-0
Guidance literature:
Multi-step reaction with 6 steps
1: 77 percent / Dibal-H / toluene / 1 h / -78 °C
2: 85 percent / I2; morpholine / toluene / 18 h / 60 °C
3: 88 percent / PCC; 4 Angstroem MS / CH2Cl2 / 20 h / 20 °C
4: 25 percent / CrCl2; NiCl2 / tetrahydrofuran / 8 h / 20 °C
5: 71 percent / DCC; DMAP / CH2Cl2 / 12 h / 20 °C
6: 46 percent / PPTS / methanol / 16 h / 20 °C
With morpholine; chromium dichloride; dmap; 4 Angstroem MS; iodine; pyridinium p-toluenesulfonate; diisobutylaluminium hydride; dicyclohexyl-carbodiimide; pyridinium chlorochromate; nickel dichloride; In tetrahydrofuran; methanol; dichloromethane; toluene; 4: Nozaki-Hiyama-Kishi reaction;
DOI:10.1016/S0040-4039(01)00708-0
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