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benzyl (S)-1-((3-(4-methoxyphenyl)isoxazol-5-yl)methylcarbamoyl)-2-methylpropyl carbamate

Base Information Edit
  • Chemical Name:benzyl (S)-1-((3-(4-methoxyphenyl)isoxazol-5-yl)methylcarbamoyl)-2-methylpropyl carbamate
  • CAS No.:1262439-64-4
  • Molecular Formula:C24H27N3O5
  • Molecular Weight:437.495
  • Hs Code.:
  • Mol file:1262439-64-4.mol
benzyl (S)-1-((3-(4-methoxyphenyl)isoxazol-5-yl)methylcarbamoyl)-2-methylpropyl carbamate

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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of benzyl (S)-1-((3-(4-methoxyphenyl)isoxazol-5-yl)methylcarbamoyl)-2-methylpropyl carbamate Edit
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Technology Process of benzyl (S)-1-((3-(4-methoxyphenyl)isoxazol-5-yl)methylcarbamoyl)-2-methylpropyl carbamate

There total 7 articles about benzyl (S)-1-((3-(4-methoxyphenyl)isoxazol-5-yl)methylcarbamoyl)-2-methylpropyl carbamate 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 2 steps
1: triphenylphosphine / tetrahydrofuran / 0 - 20 °C / Inert atmosphere
2: triethylamine / dichloromethane / 20 °C / Inert atmosphere
With triethylamine; triphenylphosphine; In tetrahydrofuran; dichloromethane; 1: Staudinger reaction / 1: Staudinger reaction;
DOI:10.1021/jm1008715
Guidance literature:
Multi-step reaction with 3 steps
1: sodium azide / N,N-dimethyl-formamide / 3 h / 20 °C / Inert atmosphere
2: triphenylphosphine / tetrahydrofuran / 0 - 20 °C / Inert atmosphere
3: triethylamine / dichloromethane / 20 °C / Inert atmosphere
With sodium azide; triethylamine; triphenylphosphine; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; 2: Staudinger reaction / 2: Staudinger reaction;
DOI:10.1021/jm1008715
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