N-α-Carbobenzyloxy-N-ε-(indole-3-acetyl)-L-lysine-p-nitrophenylester

Base Information

• Chemical Name: N-α-Carbobenzyloxy-N-ε-(indole-3-acetyl)-L-lysine-p-nitrophenylester
• CAS No.: 150151-61-4
• Molecular Formula: C₃₀H₃₀N₄O₇
• Molecular Weight: 558.591
• Mol file: 150151-61-4.mol

Synonyms:N-α-Carbobenzyloxy-N-ε-(indole-3-acetyl)-L-lysine-p-nitrophenylester

Chemical Property of N-α-Carbobenzyloxy-N-ε-(indole-3-acetyl)-L-lysine-p-nitrophenylester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of N-α-Carbobenzyloxy-N-ε-(indole-3-acetyl)-L-lysine-p-nitrophenylester

There total 1 articles about N-α-Carbobenzyloxy-N-ε-(indole-3-acetyl)-L-lysine-p-nitrophenylester 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:

Reference yield: 86.0%

indole-3-acetic acid (87-51-4) + Nα-benzyloxycarbonyl-L-lysine p-nitrophenyl ester (4272-71-3) → N-α-Carbobenzyloxy-N-ε-(indole-3-acetyl)-L-lysine-p-nitrophenylester (150151-61-4)

Guidance literature:

With pyridine; dicyclohexyl-carbodiimide; In chloroform; for 3.5h; Ambient temperature;

DOI:10.1016/0031-9422(93)85388-8

Reference yield: 87.0%

N-α-Carbobenzyloxy-N-ε-(indole-3-acetyl)-L-lysine-p-nitrophenylester (150151-61-4) → N-α-Carbobenzyloxy-N-ε-(indole-3-acetyl)-L-lysine (150151-62-5)

Guidance literature:

With sodium hydroxide; In 1,4-dioxane; water; at 0 ℃; for 1h;

DOI:10.1016/0031-9422(93)85388-8

upstream raw materials:

indole-3-acetic acid

N^α-benzyloxycarbonyl-L-lysine p-nitrophenyl ester

Downstream raw materials:

N-α-Carbobenzyloxy-N-ε-(indole-3-acetyl)-L-lysine