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2-(3-benzyloxyphenyl)-N-methyl-N-(3,4,5-trimethoxyphenethyl)acetamide

Base Information Edit
  • Chemical Name:2-(3-benzyloxyphenyl)-N-methyl-N-(3,4,5-trimethoxyphenethyl)acetamide
  • CAS No.:1277187-94-6
  • Molecular Formula:C27H31NO5
  • Molecular Weight:449.547
  • Hs Code.:
  • Mol file:1277187-94-6.mol
2-(3-benzyloxyphenyl)-N-methyl-N-(3,4,5-trimethoxyphenethyl)acetamide

Synonyms:2-(3-benzyloxyphenyl)-N-methyl-N-(3,4,5-trimethoxyphenethyl)acetamide

Suppliers and Price of 2-(3-benzyloxyphenyl)-N-methyl-N-(3,4,5-trimethoxyphenethyl)acetamide
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Chemical Property of 2-(3-benzyloxyphenyl)-N-methyl-N-(3,4,5-trimethoxyphenethyl)acetamide Edit
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Technology Process of 2-(3-benzyloxyphenyl)-N-methyl-N-(3,4,5-trimethoxyphenethyl)acetamide

There total 7 articles about 2-(3-benzyloxyphenyl)-N-methyl-N-(3,4,5-trimethoxyphenethyl)acetamide 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: sodium iodide; potassium hydroxide / ethanol / 16 h / 90 - 100 °C / Inert atmosphere
2: oxalyl dichloride; N,N-dimethyl-formamide / toluene / 1 h / 20 °C / Inert atmosphere
3: sodium hydroxide / chloroform; water / 17 h / 0 - 20 °C
With oxalyl dichloride; N,N-dimethyl-formamide; sodium iodide; potassium hydroxide; sodium hydroxide; In ethanol; chloroform; water; toluene;
DOI:10.1002/anie.201006268
Guidance literature:
Multi-step reaction with 2 steps
1: oxalyl dichloride; N,N-dimethyl-formamide / toluene / 1 h / 20 °C / Inert atmosphere
2: sodium hydroxide / chloroform; water / 17 h / 0 - 20 °C
With oxalyl dichloride; N,N-dimethyl-formamide; sodium hydroxide; In chloroform; water; toluene;
DOI:10.1002/anie.201006268
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