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N-<<<(phenylacetyl)amino>methyl>hydroxyphosphinyl>phenylalanylleucine disodium salt

Base Information
  • Chemical Name:N-<<<(phenylacetyl)amino>methyl>hydroxyphosphinyl>phenylalanylleucine disodium salt
  • CAS No.:96928-74-4
  • Molecular Formula:C24H30N3O6P*2Na
  • Molecular Weight:533.472
  • Hs Code.:
N-<<<(phenylacetyl)amino>methyl>hydroxyphosphinyl>phenylalanylleucine disodium salt

Synonyms:N-<<<(phenylacetyl)amino>methyl>hydroxyphosphinyl>phenylalanylleucine disodium salt

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Chemical Property of N-<<<(phenylacetyl)amino>methyl>hydroxyphosphinyl>phenylalanylleucine disodium salt
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Technology Process of N-<<<(phenylacetyl)amino>methyl>hydroxyphosphinyl>phenylalanylleucine disodium salt

There total 5 articles about N-<<<(phenylacetyl)amino>methyl>hydroxyphosphinyl>phenylalanylleucine disodium salt 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 hydrogen; sodium hydrogencarbonate; palladium on activated charcoal; In ethanol; water; for 1.5h; under 760 Torr;
DOI:10.1021/jm00147a015
Guidance literature:
Multi-step reaction with 5 steps
1: 94 percent / trifluoroacetic acid / 1.5 h / Ambient temperature
2: Et3N / tetrahydrofuran; CH2Cl2 / 2 h / Ambient temperature
3: 58 percent / 1N methanolic hydrazine / 72 h / Ambient temperature
4: 51 percent / pyridine / CH2Cl2 / 17 h / Ambient temperature
5: H2, NaHCO3 / 10percent Pd/C / ethanol; H2O / 1.5 h / 760 Torr
With pyridine; hydrogen; sodium hydrogencarbonate; triethylamine; trifluoroacetic acid; hydrazine; palladium on activated charcoal; In tetrahydrofuran; ethanol; dichloromethane; water;
DOI:10.1021/jm00147a015
Guidance literature:
Multi-step reaction with 4 steps
1: Et3N / tetrahydrofuran; CH2Cl2 / 2 h / Ambient temperature
2: 58 percent / 1N methanolic hydrazine / 72 h / Ambient temperature
3: 51 percent / pyridine / CH2Cl2 / 17 h / Ambient temperature
4: H2, NaHCO3 / 10percent Pd/C / ethanol; H2O / 1.5 h / 760 Torr
With pyridine; hydrogen; sodium hydrogencarbonate; triethylamine; hydrazine; palladium on activated charcoal; In tetrahydrofuran; ethanol; dichloromethane; water;
DOI:10.1021/jm00147a015
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