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2,3-benzo-10-benzyl-10-aza-1,4,7,13-tetraoxa-2-cyclopentadecene

Base Information Edit
  • Chemical Name:2,3-benzo-10-benzyl-10-aza-1,4,7,13-tetraoxa-2-cyclopentadecene
  • CAS No.:107102-14-7
  • Molecular Formula:C21H27NO4
  • Molecular Weight:357.45
  • Hs Code.:
  • Mol file:107102-14-7.mol
2,3-benzo-10-benzyl-10-aza-1,4,7,13-tetraoxa-2-cyclopentadecene

Synonyms:2,3-benzo-10-benzyl-10-aza-1,4,7,13-tetraoxa-2-cyclopentadecene

Suppliers and Price of 2,3-benzo-10-benzyl-10-aza-1,4,7,13-tetraoxa-2-cyclopentadecene
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 2,3-benzo-10-benzyl-10-aza-1,4,7,13-tetraoxa-2-cyclopentadecene Edit
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SDS file from LookChem

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Technology Process of 2,3-benzo-10-benzyl-10-aza-1,4,7,13-tetraoxa-2-cyclopentadecene

There total 3 articles about 2,3-benzo-10-benzyl-10-aza-1,4,7,13-tetraoxa-2-cyclopentadecene 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 tetrabutylammomium bromide; sodium hydroxide; In water; benzene; at 70 ℃; for 7h; Reagent/catalyst;
DOI:10.1134/S1070428012100156
Guidance literature:
Multi-step reaction with 2 steps
1: 69 percent / sodium hydroxide / H2O; tetrahydrofuran / 3 h / 0 °C
2: 32 percent / sodium hydride / tetrahydrofuran / 45 h / Heating
With sodium hydroxide; sodium hydride; In tetrahydrofuran; water;
DOI:10.1021/jo0107148
Guidance literature:
Multi-step reaction with 2 steps
1: 74 percent / sodium carbonate / acetonitrile / 9 h / Heating
2: 32 percent / sodium hydride / tetrahydrofuran / 45 h / Heating
With sodium hydride; sodium carbonate; In tetrahydrofuran; acetonitrile;
DOI:10.1021/jo0107148
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