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(9aR*,9bS*)-5a-Aza-2,5,6,7,8,9,9a,9b-octahydro-5-oxo-4-oxa-3-phenyl-1H-benzazulene

Base Information
  • Chemical Name:(9aR*,9bS*)-5a-Aza-2,5,6,7,8,9,9a,9b-octahydro-5-oxo-4-oxa-3-phenyl-1H-benzazulene
  • CAS No.:124943-97-1
  • Molecular Formula:C17H19NO2
  • Molecular Weight:269.343
  • Hs Code.:
(9aR*,9bS*)-5a-Aza-2,5,6,7,8,9,9a,9b-octahydro-5-oxo-4-oxa-3-phenyl-1H-benz<cd>azulene

Synonyms:(9aR*,9bS*)-5a-Aza-2,5,6,7,8,9,9a,9b-octahydro-5-oxo-4-oxa-3-phenyl-1H-benzazulene

Suppliers and Price of (9aR*,9bS*)-5a-Aza-2,5,6,7,8,9,9a,9b-octahydro-5-oxo-4-oxa-3-phenyl-1H-benzazulene
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of (9aR*,9bS*)-5a-Aza-2,5,6,7,8,9,9a,9b-octahydro-5-oxo-4-oxa-3-phenyl-1H-benzazulene
Chemical Property:
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Technology Process of (9aR*,9bS*)-5a-Aza-2,5,6,7,8,9,9a,9b-octahydro-5-oxo-4-oxa-3-phenyl-1H-benzazulene

There total 7 articles about (9aR*,9bS*)-5a-Aza-2,5,6,7,8,9,9a,9b-octahydro-5-oxo-4-oxa-3-phenyl-1H-benzazulene 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 6 steps
1: pyridine / CHCl3 / 12 h / Ambient temperature
2: NaI / acetone / 2 h / Heating
3: 1) LDA / 1) THF, hexane, -78 deg C 2) -78 deg C -> room temperature
4: 1) LDA / 1) THF, hexane, -78 deg C 2) -78 deg C -> room temperature
5: 1) Li(Et)3BH 2) HCl / 1) THF, -78 deg C 2) -78 deg C -> room temperature
6: 80 percent / SnCl4 / CH2Cl2 / 0.08 h / -23 °C
With pyridine; hydrogenchloride; tin(IV) chloride; lithium triethylborohydride; sodium iodide; lithium diisopropyl amide; In dichloromethane; chloroform; acetone;
DOI:10.1021/jo00292a014
Guidance literature:
Multi-step reaction with 5 steps
1: NaI / acetone / 2 h / Heating
2: 1) LDA / 1) THF, hexane, -78 deg C 2) -78 deg C -> room temperature
3: 1) LDA / 1) THF, hexane, -78 deg C 2) -78 deg C -> room temperature
4: 1) Li(Et)3BH 2) HCl / 1) THF, -78 deg C 2) -78 deg C -> room temperature
5: 80 percent / SnCl4 / CH2Cl2 / 0.08 h / -23 °C
With hydrogenchloride; tin(IV) chloride; lithium triethylborohydride; sodium iodide; lithium diisopropyl amide; In dichloromethane; acetone;
DOI:10.1021/jo00292a014
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