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N-(cyclopropylmethyl)-6,14-endo-etheno-7-(3-carboxy-3-n-butenyl)tetrahydronororipavine gamma-lactone

Base Information
  • Chemical Name:N-(cyclopropylmethyl)-6,14-endo-etheno-7-(3-carboxy-3-n-butenyl)tetrahydronororipavine gamma-lactone
  • CAS No.:127154-03-4
  • Molecular Formula:C28H31NO5
  • Molecular Weight:461.558
  • Hs Code.:
  • Mol file:127154-03-4.mol
N-(cyclopropylmethyl)-6,14-endo-etheno-7-(3-carboxy-3-n-butenyl)tetrahydronororipavine gamma-lactone

Synonyms:6,14-Ethenomorphinan,2(3H)-furanone deriv.

Suppliers and Price of N-(cyclopropylmethyl)-6,14-endo-etheno-7-(3-carboxy-3-n-butenyl)tetrahydronororipavine gamma-lactone
Supply Marketing:
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of N-(cyclopropylmethyl)-6,14-endo-etheno-7-(3-carboxy-3-n-butenyl)tetrahydronororipavine gamma-lactone
Chemical Property:
  • PSA:68.23000 
  • Density:1.41g/cm3 
  • LogP:3.20230 
Purity/Quality:
Safty Information:
  • Pictogram(s):  
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MSDS Files:

SDS file from LookChem

Useful:
Technology Process of N-(cyclopropylmethyl)-6,14-endo-etheno-7-(3-carboxy-3-n-butenyl)tetrahydronororipavine gamma-lactone

There total 7 articles about N-(cyclopropylmethyl)-6,14-endo-etheno-7-(3-carboxy-3-n-butenyl)tetrahydronororipavine gamma-lactone 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: 78 percent / NaHCO3 / dimethylformamide / 7 h / 90 °C
2: 97 percent / imidazole / dimethylformamide / 22 h
3: 22 percent / γ-MnO2 / tetrahydrofuran / 20 h
4: 84 percent / benzene / 3 h / 50 °C
5: 65 percent / activated zinc / tetrahydrofuran / 6 h / 50 °C
6: 80 percent / n-Bu4NF / tetrahydrofuran / 1.17 h
With 1H-imidazole; manganese(IV) oxide; tetrabutyl ammonium fluoride; sodium hydrogencarbonate; zinc; In tetrahydrofuran; N,N-dimethyl-formamide; benzene;
DOI:10.1021/jm00170a038
Guidance literature:
Multi-step reaction with 5 steps
1: 97 percent / imidazole / dimethylformamide / 22 h
2: 22 percent / γ-MnO2 / tetrahydrofuran / 20 h
3: 84 percent / benzene / 3 h / 50 °C
4: 65 percent / activated zinc / tetrahydrofuran / 6 h / 50 °C
5: 80 percent / n-Bu4NF / tetrahydrofuran / 1.17 h
With 1H-imidazole; manganese(IV) oxide; tetrabutyl ammonium fluoride; zinc; In tetrahydrofuran; N,N-dimethyl-formamide; benzene;
DOI:10.1021/jm00170a038
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