107569-44-8

Basic information

• Product Name: N^ε,N^ε-dimethyl-N^α-benzyloxycarbonyl-L-lysine
• Synonyms: N^ε,N^ε-dimethyl-N^α-benzyloxycarbonyl-L-lysine
• CAS NO: 107569-44-8
• Molecular Weight: 308.378
• Mol File: 107569-44-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: N^ε,N^ε-dimethyl-N^α-benzyloxycarbonyl-L-lysine(CAS DataBase Reference)
• NIST Chemistry Reference: N^ε,N^ε-dimethyl-N^α-benzyloxycarbonyl-L-lysine(107569-44-8)
• EPA Substance Registry System: N^ε,N^ε-dimethyl-N^α-benzyloxycarbonyl-L-lysine(107569-44-8)

Safety Data

• Hazardous Substances Data: 107569-44-8(Hazardous Substances Data)

Upstream product

• 50-00-0 formaldehyd 
• 2212-75-1 N₂-[(benzyloxy)carbonyl]-L-lysine 

Downstream Products

• 55528-53-5 N^ε,N^ε,N^ε-trimethyl-L-lysine dihydrochloride 
• 609367-13-7 (R)-2-[(Benzyloxy-formyl-amino)-methyl]-hexanoic acid ((S)-5-dimethylamino-1-dimethylcarbamoyl-pentyl)-amide 
• 609367-33-1 ((S)-5-Dimethylamino-1-dimethylcarbamoyl-pentyl)-carbamic acid benzyl ester 
• 13900-70-4 N^ε,N^ε,N^ε-trimethyl-N^α-benzyloxycarbonyl-L-lysine hydrochloride 
• 79416-87-8 N^ε,N^ε-dimethyl-L-lysine hydrochloride 

Relevant articles and documents

Synthesis and antifungal activity of rhodopeptin analogues. 1. Modification of the east and south amino acid moieties

(equation presented) East Amino Acid n=8, 10 South Amino Acid Synthetic Rhodopeptin Analogs Structure - activity relationships of the east and south amino acid modified analogues of rhodopeptins, novel antifungal cyclic tetrapeptides isolated from Rhodococcus species Mer-N1033, have been investigated. It was observed that a basic amino acid moiety (lysine or ornithine) as the east amino acid and a hydrophobic and bulky neutral amino acid (i.e., γ-methylleucine) as the south amino acid were indispensable structure motifs for antifungal activity of rhodopeptin analogues.