201014-19-9

Basic information

• Product Name: N-ε-2-chloro-Z-D-lysine
• Synonyms: N-ε-2-chloro-Z-D-lysine;N-e-2-chloro-Z-D-lysine;N-.EPSILON.-2-CHLORO-CBZ-D-LYSINE;(R)-2-amino-6-((2-chlorobenzyloxy)carbonylamino)hexanoic acid;H-D-Lys(2-Cl-Z)-OH N-ε-2-chloro-Z-D-lysine;N6-[[(2-Chlorophenyl)methoxy]carbonyl]-D-lysine;D-Lys(2-Cl-Z)-OH;Ne-2-Chloro-Z-D-lysine≥ 99% (TLC)
• CAS NO: 201014-19-9
• Molecular Formula: C14H19ClN2O4
• Molecular Weight: 314.767
• Mol File: 201014-19-9.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• Storage Temp.: Store at RT.
• CAS DataBase Reference: N-ε-2-chloro-Z-D-lysine(CAS DataBase Reference)
• NIST Chemistry Reference: N-ε-2-chloro-Z-D-lysine(201014-19-9)
• EPA Substance Registry System: N-ε-2-chloro-Z-D-lysine(201014-19-9)

Safety Data

• Hazardous Substances Data: 201014-19-9(Hazardous Substances Data)

Usage

Chemical Properties

White product

Upstream product

• 54613-99-9 Boc-(S)-Lys(2-Cl-Z)-OH 
• 17849-38-6 2-Chlorobenzyl alcohol 
• 75-44-5 phosgene 
• 657-27-2 L-Lysine hydrochloride 
• 39545-31-8 2-chlorobenzyl chloroformate 

Relevant articles and documents

Facile synthesis of α-hydroxy carboxylic acids from the corresponding α-amino acids

An effective and improved procedure is developed for the synthesis of α-hydroxy carboxylic acids by treatment of the corresponding protonated α-amino acid with tert-butyl nitrite in 1,4-dioxane-water. The amino moiety must be protonated and located α to a carboxylic acid function in order to undergo initial diazotization and successive hydroxylation, since neither β-amino acids nor acid derivatives such as esters and amides undergo hydroxylations. The method is successfully applied for the synthesis of 18 proteinogenic amino acids.