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Z-Lys(Tos)-Lys(Tos)-Tyr-N2H3

Base Information Edit
  • Chemical Name:Z-Lys(Tos)-Lys(Tos)-Tyr-N2H3
  • CAS No.:92398-87-3
  • Molecular Formula:C43H55N7O10S2
  • Molecular Weight:894.083
  • Hs Code.:
  • Mol file:92398-87-3.mol
Z-Lys(Tos)-Lys(Tos)-Tyr-N<sub>2</sub>H<sub>3</sub>

Synonyms:Z-Lys(Tos)-Lys(Tos)-Tyr-N2H3

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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of Z-Lys(Tos)-Lys(Tos)-Tyr-N2H3 Edit
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Technology Process of Z-Lys(Tos)-Lys(Tos)-Tyr-N2H3

There total 5 articles about Z-Lys(Tos)-Lys(Tos)-Tyr-N2H3 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 hydrazine hydrate; In methanol;
DOI:10.1021/ja00337a046
Guidance literature:
Multi-step reaction with 4 steps
1: 86 percent / Et3N, 1-hydroxybenztriazole, DCC / dimethylformamide; tetrahydrofuran
2: H2, 1 N HCl / Pd / methanol
3: 88 percent / Et3N, 1-hydroxybenztriazole, DCC / dimethylformamide
4: 98 percent / hydrazine hydrate / methanol
With hydrogenchloride; hydrogen; benzotriazol-1-ol; hydrazine hydrate; triethylamine; dicyclohexyl-carbodiimide; palladium; In tetrahydrofuran; methanol; N,N-dimethyl-formamide;
DOI:10.1021/ja00337a046
Guidance literature:
Multi-step reaction with 4 steps
1: 86 percent / Et3N, 1-hydroxybenztriazole, DCC / dimethylformamide; tetrahydrofuran
2: H2, 1 N HCl / Pd / methanol
3: 88 percent / Et3N, 1-hydroxybenztriazole, DCC / dimethylformamide
4: 98 percent / hydrazine hydrate / methanol
With hydrogenchloride; hydrogen; benzotriazol-1-ol; hydrazine hydrate; triethylamine; dicyclohexyl-carbodiimide; palladium; In tetrahydrofuran; methanol; N,N-dimethyl-formamide;
DOI:10.1021/ja00337a046
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