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Na-t-butyloxycarbonyl-L-valyl-O-acetyl-L-tyrosine N-hydroxysuccinimide ester

Base Information Edit
  • Chemical Name:Na-t-butyloxycarbonyl-L-valyl-O-acetyl-L-tyrosine N-hydroxysuccinimide ester
  • CAS No.:108305-08-4
  • Molecular Formula:C25H33N3O9
  • Molecular Weight:519.552
  • Hs Code.:
  • Mol file:108305-08-4.mol
N<sup>a</sup>-t-butyloxycarbonyl-L-valyl-O-acetyl-L-tyrosine N-hydroxysuccinimide ester

Synonyms:Na-t-butyloxycarbonyl-L-valyl-O-acetyl-L-tyrosine N-hydroxysuccinimide ester

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Chemical Property of Na-t-butyloxycarbonyl-L-valyl-O-acetyl-L-tyrosine N-hydroxysuccinimide ester Edit
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Technology Process of Na-t-butyloxycarbonyl-L-valyl-O-acetyl-L-tyrosine N-hydroxysuccinimide ester

There total 3 articles about Na-t-butyloxycarbonyl-L-valyl-O-acetyl-L-tyrosine N-hydroxysuccinimide ester 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 2 steps
1: 81 percent / 0.5N sodium bicarbonate / tetrahydrofuran / 4 h / Ambient temperature
2: 72 percent / dicyclohexylcarbodiimide / ethyl acetate
With sodium hydrogencarbonate; dicyclohexyl-carbodiimide; In tetrahydrofuran; ethyl acetate;
Guidance literature:
Multi-step reaction with 2 steps
1: 81 percent / 0.5N sodium bicarbonate / tetrahydrofuran / 4 h / Ambient temperature
2: 72 percent / dicyclohexylcarbodiimide / ethyl acetate
With sodium hydrogencarbonate; dicyclohexyl-carbodiimide; In tetrahydrofuran; ethyl acetate;
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