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2-methoxy-5-((E)-4-methyl-6-(3,3-dimethyloxiran-2-yl)hex-3-enyl)phenoxytriisopropylsilane

Base Information Edit
  • Chemical Name:2-methoxy-5-((E)-4-methyl-6-(3,3-dimethyloxiran-2-yl)hex-3-enyl)phenoxytriisopropylsilane
  • CAS No.:1507365-71-0
  • Molecular Formula:C27H46O3Si
  • Molecular Weight:446.746
  • Hs Code.:
  • Mol file:1507365-71-0.mol
2-methoxy-5-((E)-4-methyl-6-(3,3-dimethyloxiran-2-yl)hex-3-enyl)phenoxytriisopropylsilane

Synonyms:2-methoxy-5-((E)-4-methyl-6-(3,3-dimethyloxiran-2-yl)hex-3-enyl)phenoxytriisopropylsilane

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Chemical Property of 2-methoxy-5-((E)-4-methyl-6-(3,3-dimethyloxiran-2-yl)hex-3-enyl)phenoxytriisopropylsilane Edit
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Technology Process of 2-methoxy-5-((E)-4-methyl-6-(3,3-dimethyloxiran-2-yl)hex-3-enyl)phenoxytriisopropylsilane

There total 3 articles about 2-methoxy-5-((E)-4-methyl-6-(3,3-dimethyloxiran-2-yl)hex-3-enyl)phenoxytriisopropylsilane 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 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; In toluene; at 20 - 90 ℃; for 6h; Inert atmosphere;
DOI:10.1021/ol403289y
Guidance literature:
Multi-step reaction with 3 steps
1.1: silica gel; thionyl chloride / benzene / 20 °C / Inert atmosphere
2.1: n-butyllithium / tetrahydrofuran; hexane / 0 °C / Inert atmosphere
2.2: 0.5 h / Inert atmosphere
3.1: 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride / toluene / 6 h / 20 - 90 °C / Inert atmosphere
With n-butyllithium; thionyl chloride; 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; silica gel; In tetrahydrofuran; hexane; toluene; benzene;
DOI:10.1021/ol403289y
Guidance literature:
Multi-step reaction with 2 steps
1.1: n-butyllithium / tetrahydrofuran; hexane / 0 °C / Inert atmosphere
1.2: 0.5 h / Inert atmosphere
2.1: 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride / toluene / 6 h / 20 - 90 °C / Inert atmosphere
With n-butyllithium; 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; In tetrahydrofuran; hexane; toluene;
DOI:10.1021/ol403289y
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