42390-97-6

Basic information

• Product Name: H-LYS(2-CL-Z)-OH
• Synonyms: H-LYS(2-CHLORO-Z)-OH;H-LYS(2-CL-Z)-OH;H-LYS(CL-Z)-OH;L-LYSINE (2-CHLORO-CBZ);LYSINE(2-CHLORO-Z)-OH;N-EPSILON-(2-CHLORO-Z)-L-LYSINE;N-EPSILON-2-CHLORO-CARBOBENZOXY-L-LYSINE;N-ε-2-chloro-Z-L-lysine
• CAS NO: 42390-97-6
• Molecular Formula: C₁₄H₁₉ClN₂O₄
• Molecular Weight: 314.76
• Mol File: 42390-97-6.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• Storage Temp.: Store at RT.
• CAS DataBase Reference: H-LYS(2-CL-Z)-OH(CAS DataBase Reference)
• NIST Chemistry Reference: H-LYS(2-CL-Z)-OH(42390-97-6)
• EPA Substance Registry System: H-LYS(2-CL-Z)-OH(42390-97-6)

Safety Data

• Hazardous Substances Data: 42390-97-6(Hazardous Substances Data)

Usage

General Description

H-LYS(2-CL-Z)-OH is a chemical compound that consists of a lysine (Lys) amino acid with a 2-chloro-Z group attached to it. Lysine is an essential amino acid that plays a crucial role in protein synthesis and is important for overall growth and development. The addition of the 2-chloro-Z group to lysine may alter its properties and functionality, making it potentially useful for research purposes or in the development of new compounds for various applications. Further study and analysis of H-LYS(2-CL-Z)-OH are necessary to fully understand its potential uses and effects.

Upstream product

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

Downstream Products

• 73977-22-7 N^α-t-butyloxycarbonyl-N-2-chlorobenzyloxycarbonyl-L-lysine dicyclohexylammonium salt 
• 73995-35-4 Boc-Leu-Glu(OBu^t)-Gly-Pro-Pro-Gln-Lys-N2H3 
• 73995-34-3 Boc-Leu-Glu(OBu^t)-Gly-Pro-Pro-Gln-Lys-OMe 
• 73995-31-0 Boc-Pro-Pro-Gln-Lys-OMe 
• 73995-32-1 (S)-2-((S)-4-Carbamoyl-2-{[(S)-1-((S)-pyrrolidine-2-carbonyl)-pyrrolidine-2-carbonyl]-amino}-butyrylamino)-6-(2-chloro-benzyloxycarbonylamino)-hexanoic acid methyl ester 
• 73995-28-5 Boc-Gln-Lys-OMe 
• 73995-29-6 (S)-2-((S)-2-Amino-4-carbamoyl-butyrylamino)-6-(2-chloro-benzyloxycarbonylamino)-hexanoic acid methyl ester 
• 256650-50-7 Benzyl (2E,4R,5S)-9-(2-chlorophenylmethoxycarbonylamino)-4,5-[(2,4,6-trimethylphenylsulfonyl)epimino]non-2-enoate 
• 256650-46-1 (2S)-6-(2-Chlorophenylmethoxycarbonylamino)-N-methoxy-N-methyl-2-(2,4,6-trimethylphenylsulfonylamino)hexanamide 
• 256650-48-3 (3S/R,4S)-8-(2-Chlorophenylmethoxycarbonylamino)-4-(2,4,6-trimethylphenylsulfonylamino)oct-1-en-3-ol 
• 256650-49-4 (2S,3S/R)-2-[4-(2-Chlorophenylmethoxycarbonylamino)butyl]-N-(2,4,6-trimethylphenylsulfonyl)-3-vinylaziridine 
• 256650-47-2 [(S)-6-Oxo-5-(2,4,6-trimethyl-benzenesulfonylamino)-hexyl]-carbamic acid 2-chloro-benzyl ester 
• 56-87-1 L-lysine 
• 54613-99-9 Boc-(S)-Lys(2-Cl-Z)-OH 

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.