14611-35-9

Basic information

• Product Name: N^α,N^G,N^G-tri-Z-arginine p-nitrophenylester
• Synonyms: N^α,N^G,N^G-tri-Z-arginine p-nitrophenylester
• CAS NO: 14611-35-9
• Molecular Weight: 697.701
• Mol File: 14611-35-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: N^α,N^G,N^G-tri-Z-arginine p-nitrophenylester(CAS DataBase Reference)
• NIST Chemistry Reference: N^α,N^G,N^G-tri-Z-arginine p-nitrophenylester(14611-35-9)
• EPA Substance Registry System: N^α,N^G,N^G-tri-Z-arginine p-nitrophenylester(14611-35-9)

Safety Data

• Hazardous Substances Data: 14611-35-9(Hazardous Substances Data)

Upstream product

• 501-53-1 benzyl chloroformate 
• 1234-35-1 Z-Arg-OH 
• 13795-28-3 benzylpentachlorophenyl carbonate 
• 74-79-3 L-arginine 
• 100-02-7 4-nitro-phenol 
• 14611-34-8 N^α,N^δ,N^ω-tris(benzyloxycarbonyl)-L-arginine 

Downstream Products

• 80622-02-2 tris(carbobenzyloxy)-L-arginyl-N^ε-(carbobenzyloxy)-L-lysine 
• 78314-61-1 tris(benzyloxycarbonyl)-L-arginyl-L-proline 
• 271600-80-7 N^α,N^G,N^G-tribenzyloxycarbonylarginyl-arginyl-alanyl-valyl-tyrosine 
• 115692-59-6 C₅₆H₈₂N₈O₁₃ 
• 85471-58-5 H-L-Arg-L-Lys-L-Asp-L-Val-L-Tyr-OH*3HOAc 
• 127290-80-6 C₆₂H₇₃N₉O₁₇ 
• 78314-59-7 Z₃Arg-Pro-Lys(Z)-Pro-OMe 
• 78314-62-2 Z₃-Arg-Pro-Lys(Z)-Pro-OH 
• 271600-77-2 benzyl ester of N^α,N^G,N^G-tribenzyloxycarbonyl-argynyl-N-prolyl-β-benzylaspartyl-valyl-tyrosine 
• 271600-76-1 Z₃ArgGlyAsp(OBzl)ValTyrOBzl 
• 271600-75-0 Z₃ArgGlyOPfp 
• 95548-52-0 2>-thymopentin (Arg-Pro-Asp-Val-Tyr) 
• 127290-79-3 pentafluorophenyl ester of N^α,N^G,N^G-tribenzyloxycarbonylarginyl0N^ε-benzyloxycarbonyllysine 
• 61223-53-8 N^α,N^G,N^G-tribenzyloxycarbonylarginylglycine 

Relevant articles and documents

The total large-scale synthesis of argiopine

The total large-scale synthesis of a natural toxin argiopine, a polymethylenepolyamine derivative, was developed. It consisted of 26 stages and included three key block schemes. Most of the stages proceeded quantitatively, which excluded the necessity of using the chromatographic separation of intermediates.