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(benzyloxycarbonyl)-L-leucyl-L-phenylalanyl-NG-nitroargininal semicarbazone

Base Information Edit
  • Chemical Name:(benzyloxycarbonyl)-L-leucyl-L-phenylalanyl-NG-nitroargininal semicarbazone
  • CAS No.:122314-22-1
  • Molecular Formula:C30H42N10O7
  • Molecular Weight:654.726
  • Hs Code.:
  • Mol file:122314-22-1.mol
(benzyloxycarbonyl)-L-leucyl-L-phenylalanyl-N<sup>G</sup>-nitroargininal semicarbazone

Synonyms:(benzyloxycarbonyl)-L-leucyl-L-phenylalanyl-NG-nitroargininal semicarbazone

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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of (benzyloxycarbonyl)-L-leucyl-L-phenylalanyl-NG-nitroargininal semicarbazone Edit
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Technology Process of (benzyloxycarbonyl)-L-leucyl-L-phenylalanyl-NG-nitroargininal semicarbazone

There total 2 articles about (benzyloxycarbonyl)-L-leucyl-L-phenylalanyl-NG-nitroargininal semicarbazone 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 triethylamine; In N,N-dimethyl-formamide; at 0 ℃; for 3h; Yield given;
DOI:10.1021/jm00163a014
Guidance literature:
Multi-step reaction with 2 steps
1: 1.) Et3N / 1.) DMF, -15 deg C, 30 min, 2.) DMF, -15 deg C, 45 min
2: triethylamine / dimethylformamide / a) 0 deg C, 4 h, b) RT, overnight
With triethylamine; In N,N-dimethyl-formamide;
DOI:10.1021/jm00060a016
Guidance literature:
With hydrogenchloride; hydrogen; palladium on activated charcoal; In methanol; for 18h;
DOI:10.1021/jm00163a014
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