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Nα-diphenylphosphinoylphenylalanylphenylalanylvalylphenylalanine amide

Base Information
  • Chemical Name:Nα-diphenylphosphinoylphenylalanylphenylalanylvalylphenylalanine amide
  • CAS No.:96886-64-5
  • Molecular Formula:C44H48N5O5P
  • Molecular Weight:757.869
  • Hs Code.:
N<sub>α</sub>-diphenylphosphinoylphenylalanylphenylalanylvalylphenylalanine amide

Synonyms:Nα-diphenylphosphinoylphenylalanylphenylalanylvalylphenylalanine amide

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Chemical Property of Nα-diphenylphosphinoylphenylalanylphenylalanylvalylphenylalanine amide
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Technology Process of Nα-diphenylphosphinoylphenylalanylphenylalanylvalylphenylalanine amide

There total 17 articles about Nα-diphenylphosphinoylphenylalanylphenylalanylvalylphenylalanine amide 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 8 steps
1: 75 percent / 4M aq. NaOH, 1M aq. NaHCO3 / 18 h / Ambient temperature
2: 83 percent / DCCI, ammonium salt of hydroxybenzotriazole / CH2Cl2 / Ambient temperature
3: 96 percent / H2 / 10percent Pd/C / dimethylformamide / 18 h / Ambient temperature
4: CH2Cl2; dimethylformamide / 0.67 h / 0 °C
5: 90 percent / 10M methanolic HCl / methanol; CDCl3 / 1.67 h / 0 °C
6: N-methylmorpholine / CH2Cl2; dimethylformamide / 0.5 h / 0 °C
7: 90 percent / 10M methanolic HCl / methanol / 1.58 h / 0 °C
8: N-methylmorpholine / CH2Cl2; dimethylformamide / 0.5 h / 0 °C
With 4-methyl-morpholine; hydrogenchloride; sodium hydroxide; ammonium salt of hydroxybenzotriazole; hydrogen; sodium hydrogencarbonate; dicyclohexyl-carbodiimide; palladium on activated charcoal; In methanol; chloroform-d1; dichloromethane; N,N-dimethyl-formamide;
Guidance literature:
Multi-step reaction with 7 steps
1: 83 percent / DCCI, ammonium salt of hydroxybenzotriazole / CH2Cl2 / Ambient temperature
2: 96 percent / H2 / 10percent Pd/C / dimethylformamide / 18 h / Ambient temperature
3: CH2Cl2; dimethylformamide / 0.67 h / 0 °C
4: 90 percent / 10M methanolic HCl / methanol; CDCl3 / 1.67 h / 0 °C
5: N-methylmorpholine / CH2Cl2; dimethylformamide / 0.5 h / 0 °C
6: 90 percent / 10M methanolic HCl / methanol / 1.58 h / 0 °C
7: N-methylmorpholine / CH2Cl2; dimethylformamide / 0.5 h / 0 °C
With 4-methyl-morpholine; hydrogenchloride; ammonium salt of hydroxybenzotriazole; hydrogen; dicyclohexyl-carbodiimide; palladium on activated charcoal; In methanol; chloroform-d1; dichloromethane; N,N-dimethyl-formamide;
Guidance literature:
Multi-step reaction with 6 steps
1: 96 percent / H2 / 10percent Pd/C / dimethylformamide / 18 h / Ambient temperature
2: CH2Cl2; dimethylformamide / 0.67 h / 0 °C
3: 90 percent / 10M methanolic HCl / methanol; CDCl3 / 1.67 h / 0 °C
4: N-methylmorpholine / CH2Cl2; dimethylformamide / 0.5 h / 0 °C
5: 90 percent / 10M methanolic HCl / methanol / 1.58 h / 0 °C
6: N-methylmorpholine / CH2Cl2; dimethylformamide / 0.5 h / 0 °C
With 4-methyl-morpholine; hydrogenchloride; hydrogen; palladium on activated charcoal; In methanol; chloroform-d1; dichloromethane; N,N-dimethyl-formamide;
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