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trans-7-hexyl-2-phenyl-3-(triethylsiloxy)oxepane

Base Information
  • Chemical Name:trans-7-hexyl-2-phenyl-3-(triethylsiloxy)oxepane
  • CAS No.:128372-43-0
  • Molecular Formula:C24H42O2Si
  • Molecular Weight:390.682
  • Hs Code.:
trans-7-hexyl-2-phenyl-3-(triethylsiloxy)oxepane

Synonyms:

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Chemical Property of trans-7-hexyl-2-phenyl-3-(triethylsiloxy)oxepane
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Technology Process of trans-7-hexyl-2-phenyl-3-(triethylsiloxy)oxepane

There total 17 articles about trans-7-hexyl-2-phenyl-3-(triethylsiloxy)oxepane 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 8 steps
1: 1) butyllithium / 1) -78 deg C, 30 min, THF, 2a) -78 deg C, 1 h, 2b) 0 deg C, 2 h
2: 1) LDA / 1) -78 deg C, 30 min, 2) -78 deg C -> room temperature
3: methanesulphonyl azide, triethylamine / ethanol / 60 h / Ambient temperature
4: 81 percent / hydrochloric acid / tetrahydrofuran / 0.08 h
5: 73 percent / dirhodium tetraacetate / benzene / 0.08 h / Heating
6: 97 percent / cerium trichloride, sodium borohydride / methanol / 0.08 h / Ambient temperature
7: 61 percent / 2,6-dimethylpyridine / CH2Cl2 / 0.5 h / Ambient temperature
8: 1) magnesium, zinc bromide / 1) THF, room temperature, 30 min, 2) room temperature, overnight
With 2,6-dimethylpyridine; hydrogenchloride; dirhodium tetraacetate; sodium tetrahydroborate; n-butyllithium; cerium(III) chloride; magnesium; triethylamine; Methanesulfonyl azide; zinc dibromide; lithium diisopropyl amide; In tetrahydrofuran; methanol; ethanol; dichloromethane; benzene;
Guidance literature:
Multi-step reaction with 7 steps
1: 1) LDA / 1) -78 deg C, 30 min, 2) -78 deg C -> room temperature
2: methanesulphonyl azide, triethylamine / ethanol / 60 h / Ambient temperature
3: 81 percent / hydrochloric acid / tetrahydrofuran / 0.08 h
4: 73 percent / dirhodium tetraacetate / benzene / 0.08 h / Heating
5: 97 percent / cerium trichloride, sodium borohydride / methanol / 0.08 h / Ambient temperature
6: 61 percent / 2,6-dimethylpyridine / CH2Cl2 / 0.5 h / Ambient temperature
7: 1) magnesium, zinc bromide / 1) THF, room temperature, 30 min, 2) room temperature, overnight
With 2,6-dimethylpyridine; hydrogenchloride; dirhodium tetraacetate; sodium tetrahydroborate; cerium(III) chloride; magnesium; triethylamine; Methanesulfonyl azide; zinc dibromide; lithium diisopropyl amide; In tetrahydrofuran; methanol; ethanol; dichloromethane; benzene;
Guidance literature:
Multi-step reaction with 2 steps
1: 61 percent / 2,6-dimethylpyridine / CH2Cl2 / 0.5 h / Ambient temperature
2: 1) magnesium, zinc bromide / 1) THF, room temperature, 30 min, 2) room temperature, overnight
With 2,6-dimethylpyridine; magnesium; zinc dibromide; In dichloromethane;
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