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Hexanal, 6-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-3-[(4-methoxyphenyl)methoxy]-2- methyl-, (2S,3R)-

Base Information Edit
  • Chemical Name:Hexanal, 6-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-3-[(4-methoxyphenyl)methoxy]-2- methyl-, (2S,3R)-
  • CAS No.:479673-40-0
  • Molecular Formula:C21H36O4Si
  • Molecular Weight:380.6
  • Hs Code.:
  • Mol file:479673-40-0.mol
Hexanal,
6-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-3-[(4-methoxyphenyl)methoxy]-2-
methyl-, (2S,3R)-

Synonyms:

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Chemical Property of Hexanal, 6-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-3-[(4-methoxyphenyl)methoxy]-2- methyl-, (2S,3R)- Edit
Chemical Property:
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Technology Process of Hexanal, 6-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-3-[(4-methoxyphenyl)methoxy]-2- methyl-, (2S,3R)-

There total 7 articles about Hexanal, 6-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-3-[(4-methoxyphenyl)methoxy]-2- methyl-, (2S,3R)- 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 sulfur trioxide pyridine complex; N-ethyl-N,N-diisopropylamine; In dichloromethane; dimethyl sulfoxide; at 20 ℃; for 1h;
DOI:10.1021/jm0204136
Guidance literature:
Multi-step reaction with 5 steps
1: 95 percent / lithium borohydride / methanol; tetrahydrofuran / 2.33 h / 0 - 20 °C
2: 72 percent / pyridinium p-toluenesulfonate / benzene / 15 h / Heating
3: diisobutylaluminum hydride / tetrahydrofuran; CH2Cl2 / 1 h / 0 °C
4: pyridinium sulfur trioxide; diisopropylethylamine / dimethylsulfoxide; CH2Cl2 / 1 h / 20 °C
With lithium borohydride; sulfur trioxide pyridine complex; pyridinium p-toluenesulfonate; diisobutylaluminium hydride; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; methanol; dichloromethane; dimethyl sulfoxide; benzene; 1: Evans syn-aldol condensation;
DOI:10.1021/jm0204136
Guidance literature:
Multi-step reaction with 7 steps
1: 95 percent / pyridinium sulfur trioxide
2: 95 percent / lithium borohydride / methanol; tetrahydrofuran / 2.33 h / 0 - 20 °C
3: 72 percent / pyridinium p-toluenesulfonate / benzene / 15 h / Heating
4: diisobutylaluminum hydride / tetrahydrofuran; CH2Cl2 / 1 h / 0 °C
5: pyridinium sulfur trioxide; diisopropylethylamine / dimethylsulfoxide; CH2Cl2 / 1 h / 20 °C
With lithium borohydride; sulfur trioxide pyridine complex; pyridinium p-toluenesulfonate; diisobutylaluminium hydride; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; methanol; dichloromethane; dimethyl sulfoxide; benzene; 3: Evans syn-aldol condensation;
DOI:10.1021/jm0204136
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