870450-04-7

Basic information

• Product Name: 3-Pyridinecarboxylic acid, 6-[[[(1S)-1-[[(methylsulfonyl)oxy]methyl]-2-[4-(phenylmethoxy)phenyl]ethyl ]amino]carbonyl]-, methyl ester
• CAS NO: 870450-04-7
• Molecular Formula: C25H26N2O7S
• Molecular Weight: 498.557
• Mol File: 870450-04-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3-Pyridinecarboxylic acid, 6-[[[(1S)-1-[[(methylsulfonyl)oxy]methyl]-2-[4-(phenylmethoxy)phenyl]ethyl ]amino]carbonyl]-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Pyridinecarboxylic acid, 6-[[[(1S)-1-[[(methylsulfonyl)oxy]methyl]-2-[4-(phenylmethoxy)phenyl]ethyl ]amino]carbonyl]-, methyl ester(870450-04-7)
• EPA Substance Registry System: 3-Pyridinecarboxylic acid, 6-[[[(1S)-1-[[(methylsulfonyl)oxy]methyl]-2-[4-(phenylmethoxy)phenyl]ethyl ]amino]carbonyl]-, methyl ester(870450-04-7)

Safety Data

• Hazardous Substances Data: 870450-04-7(Hazardous Substances Data)

Upstream product

• 870450-03-6 6-[(S)-2-(4-Benzyloxy-phenyl)-1-hydroxymethyl-ethylcarbamoyl]-nicotinic acid methyl ester 
• 124-63-0 methanesulfonyl chloride 
• 17874-79-2 pyridine-2,5-dicarboxylic acid 5-methyl ester 
• 169124-35-0 6-chlorocarbonyl-nicotinic acid methyl ester 
• 66605-58-1 O-benzyl N-Boc-L-tyrosinol 
• 85803-44-7 (S)-2-amino-3-(4-benzyloxyphenyl)-1-propanol 
• 60-18-4 L-tyrosine 
• 4326-36-7 (S)-N-(tert-butoxycarbonyl)tyrosine methyl ester 
• 27513-44-6 N-tert-butoxycarbonyl-O-benzyl-(S)-tyrosine methyl ester 
• 1080-06-4 L-Tyr-OMe 
• 881-86-7 dimethyl 2,5-pyridine dicarboxylate 
• 100-26-5 Pyridine-2,5-dicarboxylic acid 

Relevant articles and documents

Ligand creation via linking - A rapid and convenient method for construction of novel supported PyOX-ligands

A novel supported amino alcohol linker was synthesized and utilized for attachment of picolinic acid derivatives onto different supports. When the resin bound molecule was further activated, the PyOX-moiety could be constructed reliably in enantiopure form. Furthermore, an efficient Pd-catalyzed modification of a picolinic acid derivative is presented.