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11b-phenyl-1,2,3,5,6,11b-hexahydro<1>benzothieno<3,2-g>indolizine

Base Information Edit
  • Chemical Name:11b-phenyl-1,2,3,5,6,11b-hexahydro<1>benzothieno<3,2-g>indolizine
  • CAS No.:99659-37-7
  • Molecular Formula:C20H19NS
  • Molecular Weight:305.444
  • Hs Code.:
  • Mol file:99659-37-7.mol
11b-phenyl-1,2,3,5,6,11b-hexahydro<1>benzothieno<3,2-g>indolizine

Synonyms:11b-phenyl-1,2,3,5,6,11b-hexahydro<1>benzothieno<3,2-g>indolizine

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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 11b-phenyl-1,2,3,5,6,11b-hexahydro<1>benzothieno<3,2-g>indolizine Edit
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Technology Process of 11b-phenyl-1,2,3,5,6,11b-hexahydro<1>benzothieno<3,2-g>indolizine

There total 4 articles about 11b-phenyl-1,2,3,5,6,11b-hexahydro<1>benzothieno<3,2-g>indolizine 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 lithium aluminium tetrahydride; In tetrahydrofuran; for 8h; Heating;
DOI:10.1071/CH9850765
Guidance literature:
Multi-step reaction with 3 steps
1: 89 percent / CH2Cl2 / 7 h / 0 - 5 °C
2: 82 percent / 85percent orthophosphoric acid / 1 h / 95 - 105 °C
3: 89 percent / lithium tetrahydroaluminate / tetrahydrofuran / 8 h / Heating
With lithium aluminium tetrahydride; phosphoric acid; In tetrahydrofuran; dichloromethane;
DOI:10.1071/CH9850765
Guidance literature:
Multi-step reaction with 3 steps
1: 89 percent / CH2Cl2 / 7 h / 0 - 5 °C
2: 82 percent / 85percent orthophosphoric acid / 1 h / 95 - 105 °C
3: 89 percent / lithium tetrahydroaluminate / tetrahydrofuran / 8 h / Heating
With lithium aluminium tetrahydride; phosphoric acid; In tetrahydrofuran; dichloromethane;
DOI:10.1071/CH9850765
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