1228178-53-7

Basic information

• Product Name: Fmoc-Ser(Bzl)-Gly-ψ(NH-CO-NH)-Ala-OBzl
• Synonyms: Fmoc-Ser(Bzl)-Gly-ψ(NH-CO-NH)-Ala-OBzl
• CAS NO: 1228178-53-7
• Molecular Weight: 650.731
• Mol File: 1228178-53-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Fmoc-Ser(Bzl)-Gly-ψ(NH-CO-NH)-Ala-OBzl(CAS DataBase Reference)
• NIST Chemistry Reference: Fmoc-Ser(Bzl)-Gly-ψ(NH-CO-NH)-Ala-OBzl(1228178-53-7)
• EPA Substance Registry System: Fmoc-Ser(Bzl)-Gly-ψ(NH-CO-NH)-Ala-OBzl(1228178-53-7)

Safety Data

• Hazardous Substances Data: 1228178-53-7(Hazardous Substances Data)

Upstream product

• 1228178-31-1 C₃₁H₃₀N₄O₈ 
• 42854-62-6 L-alanine benzyl ester p-toluenesulfonate 

Relevant articles and documents

An efficient concomitant synthesis of O-succinimidyl-(9H-fluoren-9-yl methoxy arbonylamino)peptidyl carbamates and their application in the synthesis of oligo-α-peptidyl ureas

An efficient method for the synthesis of O-succinimidyl (9H-fluorene-9-yl methoxycarbonylamine) peptidyl carbamates from the corresponding N α-Fmoc peptidyl isocyanates through the concomitant Curtius rearrangement of NαFmoc peptidyl acid azide and coupling with N-hydroxysuccinimide is described. The introduction of urea moiety at various positions in peptidyl backbone of VALVAL hexapeptide sequence has been carried out by the fragment coupling using peptidyl carbamates. All the oligo-a-peptidyl ureas are isolated as crystalline solids in 80-85% yield and have been fully characterized by 1H and 13C NMR and mass spectrometry.