103144-79-2

Basic information

• Product Name: L-Leucine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]glycyl-L-phenylalanyl-
• CAS NO: 103144-79-2
• Molecular Formula: C32H35N3O6
• Molecular Weight: 557.646
• Mol File: 103144-79-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: L-Leucine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]glycyl-L-phenylalanyl-(CAS DataBase Reference)
• NIST Chemistry Reference: L-Leucine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]glycyl-L-phenylalanyl-(103144-79-2)
• EPA Substance Registry System: L-Leucine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]glycyl-L-phenylalanyl-(103144-79-2)

Safety Data

• Hazardous Substances Data: 103144-79-2(Hazardous Substances Data)

Upstream product

• 28920-43-6 (fluorenylmethoxy)carbonyl chloride 
• 15373-56-5 glycyl-L-phenylalanyl-L-leucine 
• 29022-11-5 N-(fluoren-9-ylmethoxycarbonyl)glycine 
• 35661-60-0 Fmoc-Leu-OH 
• 35661-40-6 N-Fmoc L-Phe 

Downstream Products

• 160036-37-3 (S)-2-{(S)-2-[2-(9H-Fluoren-9-ylmethoxycarbonylamino)-acetylamino]-3-phenyl-propionylamino}-4-methyl-pentanoic acid pentafluorophenyl ester 

Relevant articles and documents

CATALYTIC ASYMMETRIC SYNTHESIS OF PEPTIDES ON POLYMER SUPPORT

A novel approach to the synthesis of peptides through the catalytic asymmetric hydrogenation of dehydrotripeptides linked to the Wang resin, using rhodium complexes with chiral diphosphine ligands as the catalysts, is described

Synthesis of peptide derivatives of 5-fluorouracil

The preparation of di-, tetra- and pentapeptides carrying 5-fluorouracil as an α-substituent of a terminal glycine moiety is described. The dipeptide compounds were synthetized by addition of ethyl glyoxylate to N-(benzyl-oxycarbonyl)-amino acid amides, s