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(2Z,4E,8Z,10E)-N-isobutyldodeca-2,4,8,10-tetraenamide

Base Information Edit
  • Chemical Name:(2Z,4E,8Z,10E)-N-isobutyldodeca-2,4,8,10-tetraenamide
  • CAS No.:1308271-58-0
  • Molecular Formula:C16H25NO
  • Molecular Weight:247.381
  • Hs Code.:
  • Mol file:1308271-58-0.mol
(2Z,4E,8Z,10E)-N-isobutyldodeca-2,4,8,10-tetraenamide

Synonyms:(2Z,4E,8Z,10E)-N-isobutyldodeca-2,4,8,10-tetraenamide

Suppliers and Price of (2Z,4E,8Z,10E)-N-isobutyldodeca-2,4,8,10-tetraenamide
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of (2Z,4E,8Z,10E)-N-isobutyldodeca-2,4,8,10-tetraenamide Edit
Chemical Property:
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Technology Process of (2Z,4E,8Z,10E)-N-isobutyldodeca-2,4,8,10-tetraenamide

There total 12 articles about (2Z,4E,8Z,10E)-N-isobutyldodeca-2,4,8,10-tetraenamide 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:
2-N-iso-butyl-2-oxoethyl phosphonium chloride; With potassium tert-butylate; In tetrahydrofuran; at 20 ℃; for 0.5h;
C10H14O; In tetrahydrofuran; at 0 ℃; for 2h;
DOI:10.1021/jo200289f
Guidance literature:
Multi-step reaction with 3 steps
1.1: naphthalene; lithium; zinc(II) chloride / tetrahydrofuran; methanol / 50 °C
2.1: oxalyl dichloride; dimethyl sulfoxide / dichloromethane / -78 - -10 °C
2.2: -78 - 20 °C
3.1: potassium tert-butylate / tetrahydrofuran / 0.5 h / 20 °C
3.2: 2 h / 0 °C
With oxalyl dichloride; naphthalene; potassium tert-butylate; lithium; dimethyl sulfoxide; zinc(II) chloride; In tetrahydrofuran; methanol; dichloromethane; 2.1: Swern oxidation / 2.2: Swern oxidation / 3.1: Wittig reaction / 3.2: Wittig reaction;
DOI:10.1021/jo200289f
Guidance literature:
Multi-step reaction with 2 steps
1.1: oxalyl dichloride; dimethyl sulfoxide / dichloromethane / -78 - -10 °C
1.2: -78 - 20 °C
2.1: potassium tert-butylate / tetrahydrofuran / 0.5 h / 20 °C
2.2: 2 h / 0 °C
With oxalyl dichloride; potassium tert-butylate; dimethyl sulfoxide; In tetrahydrofuran; dichloromethane; 1.1: Swern oxidation / 1.2: Swern oxidation / 2.1: Wittig reaction / 2.2: Wittig reaction;
DOI:10.1021/jo200289f
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