161453-37-8

Basic information

• Product Name: BOC-BETA-(2-QUINOLYL)-ALA-OH
• Synonyms: (2S)-3-isoquinolin-3-yl-2-[(2-Methylpropan-2-yl)oxycarbonylaMino]propanoic acid;Boc-(S)-2-Amino-3-quinolin-2-yl-propionic acid;Boc-3-(2'-quinolyl)-L-alanine≥ 99% (TLC);Boc-L-Ala(2'-quinolyl)-OH;L-BOC-BETA-(2-QUINOLYL)-ALA-OH;BOC-QAL(2)-OH;BOC-L-2-QUINOYLALANINE;BOC-ALA(2'-QUINOLYL)-OH
• CAS NO: 161453-37-8
• Molecular Formula: C17H20N2O4
• Molecular Weight: 316.35
• Mol File: 161453-37-8.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: BOC-BETA-(2-QUINOLYL)-ALA-OH(CAS DataBase Reference)
• NIST Chemistry Reference: BOC-BETA-(2-QUINOLYL)-ALA-OH(161453-37-8)
• EPA Substance Registry System: BOC-BETA-(2-QUINOLYL)-ALA-OH(161453-37-8)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 161453-37-8(Hazardous Substances Data)

Usage

Chemical Properties

White powder

Upstream product

• 123-91-1 1,4-dioxane 
• 210420-41-0 N-Acetyl-β-(2-quinolyl)-L-alanine 
• 24424-99-5 di-tert-butyl dicarbonate 
• 161453-32-3 (2S,5S)-(+)-5-(2'-quinolylmethyl)-2-tert-butyl-1-tert-butoxycarbonyl-3-methyl-4-imidazolidinone 
• 161513-46-8 (S)-(+)-2-amino-3-(2'-quinolyl)propionic acid 

Relevant articles and documents

Boronic ester and acid compounds, synthesis and uses

Disclosed herein are boronic ester and acid compounds, their synthesis and uses. More specifically, disclosed herein is a method for reducing the rate of degradation of proteins in an animal comprising contacting cells of the animal with certain boronic ester and acid compounds.

Intercalator amino acids: Synthesis of heteroaryl alanines

Stereoselective alkylation of (S)-(-)-2-t-butyl-1-t-butyloxycarbonyl-3-methyl-4-imidazolinone with 2-chloromethylquinoline, 2-chloromethylquinoxaline and 5-chloromethyl-1,10-phenanthroline, followed by hydrolysis, afforded the corresponding (S)-(+)-α-amino acids with high enantiomeric excess.