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Aloc-D-Ala-Phe-Lys(Aloc)-p-aminobenzyl oxycarbonyl p-nitrophenyl carbonate

Base Information Edit
  • Chemical Name:Aloc-D-Ala-Phe-Lys(Aloc)-p-aminobenzyl oxycarbonyl p-nitrophenyl carbonate
  • CAS No.:253863-34-2
  • Molecular Formula:C40H46N6O12
  • Molecular Weight:802.838
  • Hs Code.:
  • Mol file:253863-34-2.mol
Aloc-D-Ala-Phe-Lys(Aloc)-p-aminobenzyl oxycarbonyl p-nitrophenyl carbonate

Synonyms:Aloc-D-Ala-Phe-Lys(Aloc)-p-aminobenzyl oxycarbonyl p-nitrophenyl carbonate

Suppliers and Price of Aloc-D-Ala-Phe-Lys(Aloc)-p-aminobenzyl oxycarbonyl p-nitrophenyl carbonate
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
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  • Chemicals and raw materials
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Total 2 raw suppliers
Chemical Property of Aloc-D-Ala-Phe-Lys(Aloc)-p-aminobenzyl oxycarbonyl p-nitrophenyl carbonate Edit
Chemical Property:
Purity/Quality:

97% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of Aloc-D-Ala-Phe-Lys(Aloc)-p-aminobenzyl oxycarbonyl p-nitrophenyl carbonate

There total 13 articles about Aloc-D-Ala-Phe-Lys(Aloc)-p-aminobenzyl oxycarbonyl p-nitrophenyl carbonate 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 3 steps
1: N-methylmorpholine / tetrahydrofuran / 3 h / -40 - -30 °C
2: N-methylmorpholine / tetrahydrofuran / 2 h
3: 67 percent / pyridine / tetrahydrofuran; CH2Cl2 / 48 h / 20 °C
With 4-methyl-morpholine; pyridine; In tetrahydrofuran; dichloromethane; 1: Substitution / 2: Substitution / 3: Substitution;
DOI:10.1021/jm9910472
Guidance literature:
Multi-step reaction with 8 steps
1: 89 percent / Et3N / CH2Cl2 / 5 h / 20 °C
2: 2N aq. NaOH / dioxane; methanol / 1 h / 20 °C
3: Et3N / CH2Cl2 / 16 h
4: HCl / ethyl acetate / 5 h
5: 86 percent / Et3N / H2O; acetonitrile / pH 3 - 9.5
6: N-methylmorpholine / tetrahydrofuran / 3 h / -40 - -30 °C
7: N-methylmorpholine / tetrahydrofuran / 2 h
8: 67 percent / pyridine / tetrahydrofuran; CH2Cl2 / 48 h / 20 °C
With 4-methyl-morpholine; pyridine; hydrogenchloride; sodium hydroxide; triethylamine; In tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane; water; ethyl acetate; acetonitrile; 1: Substitution / 2: Hydrolysis / 3: Substitution / 4: Hydrolysis / 5: Substitution / 6: Substitution / 7: Substitution / 8: Substitution;
DOI:10.1021/jm9910472
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