10342-52-6

Basic information

• Product Name: N^α-Benzyloxycarbonyl-N^ε-tert-butyloxycarbonyl-L-lysylglycine Methyl Ester
• Synonyms: N^α-Benzyloxycarbonyl-N^ε-tert-butyloxycarbonyl-L-lysylglycine Methyl Ester
• CAS NO: 10342-52-6
• Molecular Weight: 451.52
• Mol File: 10342-52-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: N^α-Benzyloxycarbonyl-N^ε-tert-butyloxycarbonyl-L-lysylglycine Methyl Ester(CAS DataBase Reference)
• NIST Chemistry Reference: N^α-Benzyloxycarbonyl-N^ε-tert-butyloxycarbonyl-L-lysylglycine Methyl Ester(10342-52-6)
• EPA Substance Registry System: N^α-Benzyloxycarbonyl-N^ε-tert-butyloxycarbonyl-L-lysylglycine Methyl Ester(10342-52-6)

Safety Data

• Hazardous Substances Data: 10342-52-6(Hazardous Substances Data)

Upstream product

• 2389-60-8 Z-Lys(Boc)-OH 
• 5680-79-5 glycine ethyl ester hydrochloride 
• 2212-76-2 N^α-benzyloxycarbonyl-N^ε-tert-butyloxycarbonyl-L-lysine dicyclohexylamine salt 
• 616-34-2 methoxycarbonylmethylamine 
• 24424-99-5 di-tert-butyl dicarbonate 
• 2212-75-1 N₂-[(benzyloxy)carbonyl]-L-lysine 

Downstream Products

• 87136-46-7 N^α-Benzyloxycarbonyl-N^ε-tert-butyloxycarbonyl-L-lysylglycyl-L-asparaginyl-L-leucine Lithium Salt 
• 87136-45-6 N^α-Benzyloxycarbonyl-N^ε-tert-butyloxycarbonyl-L-lysylglycyl-L-asparaginyl-L-leucine Methyl Ester 
• 101250-76-4 Z-Pro-Lys(BOC)-Gly-OH 
• 101249-85-8 N--L-prolyl>-L-lysyl>glycine ditrifluoroacetate 
• 101249-83-6 methyl N-6-<(1,1-dimethylethoxy)carbonyl>-N²-<1-<(phenylmethoxy)carbonyl>-L-prolyl>-L-lysyl>glycinate 
• 211797-31-8 ((S)-6-Amino-2-benzyloxycarbonylamino-hexanoylamino)-acetic acid methyl ester 
• 47689-13-4 N-(N^α-carbobenzoxy-N^ε-tert-butoxycarbonyl-L-lysyl)glycine 

Relevant articles and documents

Binding of a hemoregulatory tetrapeptide by a bis-guanidinium crown ether

A synthetic receptor for the molecular recognition of a tetrapeptide in aqueous buffer was obtained by combining a luminescent crown ether with two pyrrole-guanidinium moieties. The compound interacts with ammonium carboxylates of complementary geometry a

Synthetic Studies on Sequences of Vitamin K Dependent Proteins. Gla-Arg-Gla Sequences

The synthesis of peptides containing the Gla-Arg-Gla sequence is reported.Nuclear magnetic resonance studies suggest that intramolecular salt bridge interactions occur between the guanidino group of arginine and the γ-carboxyglutamic acid.