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(8S,9S)-9-L-tyrosinylamide(9-deoxy)-epi-cinchonidine

Base Information
  • Chemical Name:(8S,9S)-9-L-tyrosinylamide(9-deoxy)-epi-cinchonidine
  • CAS No.:1620137-44-1
  • Molecular Formula:C28H32N4O2
  • Molecular Weight:456.588
  • Hs Code.:
(8S,9S)-9-L-tyrosinylamide(9-deoxy)-epi-cinchonidine

Synonyms:(8S,9S)-9-L-tyrosinylamide(9-deoxy)-epi-cinchonidine

Suppliers and Price of (8S,9S)-9-L-tyrosinylamide(9-deoxy)-epi-cinchonidine
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 (8S,9S)-9-L-tyrosinylamide(9-deoxy)-epi-cinchonidine
Chemical Property:
Purity/Quality:
Safty Information:
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Technology Process of (8S,9S)-9-L-tyrosinylamide(9-deoxy)-epi-cinchonidine

There total 6 articles about (8S,9S)-9-L-tyrosinylamide(9-deoxy)-epi-cinchonidine 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 piperidine; In N,N-dimethyl-formamide;
DOI:10.1016/j.tetasy.2014.05.003
Guidance literature:
Multi-step reaction with 3 steps
1: triphenylphosphine / tetrahydrofuran / 4 h / 48 - 52 °C
2: tetrahydrofuran / 1 h / 20 °C
3: piperidine / N,N-dimethyl-formamide
With piperidine; triphenylphosphine; In tetrahydrofuran; N,N-dimethyl-formamide; 1: |Staudinger Azide Reduction;
DOI:10.1016/j.tetasy.2014.05.003
Guidance literature:
Multi-step reaction with 4 steps
1: sodium azide / N,N-dimethyl-formamide / 24 h / 80 °C
2: triphenylphosphine / tetrahydrofuran / 4 h / 48 - 52 °C
3: tetrahydrofuran / 1 h / 20 °C
4: piperidine / N,N-dimethyl-formamide
With piperidine; sodium azide; triphenylphosphine; In tetrahydrofuran; N,N-dimethyl-formamide; 2: |Staudinger Azide Reduction;
DOI:10.1016/j.tetasy.2014.05.003
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