909913-51-5

Basic information

• Product Name: (2S,3S,4S)-2-amino-4-[2-(5-benzyloxypyridyl)]-3-methyl-butano-4-lactone
• Synonyms: (2S,3S,4S)-2-amino-4-[2-(5-benzyloxypyridyl)]-3-methyl-butano-4-lactone
• CAS NO: 909913-51-5
• Molecular Weight: 298.342
• Mol File: 909913-51-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2S,3S,4S)-2-amino-4-[2-(5-benzyloxypyridyl)]-3-methyl-butano-4-lactone(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,3S,4S)-2-amino-4-[2-(5-benzyloxypyridyl)]-3-methyl-butano-4-lactone(909913-51-5)
• EPA Substance Registry System: (2S,3S,4S)-2-amino-4-[2-(5-benzyloxypyridyl)]-3-methyl-butano-4-lactone(909913-51-5)

Safety Data

• Hazardous Substances Data: 909913-51-5(Hazardous Substances Data)

Upstream product

• 100-39-0 benzyl bromide 
• 59781-11-2 (5-(benzyloxy)pyridin-2-yl)methanol 
• 59781-08-7 5-benzyloxypyridin-2-carbaldehyde 
• 63793-98-6 5-benzyloxy-2-methyl-pyridine 
• 1121-78-4 5-Hydroxy-2-methylpyridine 
• 909913-44-6 (2S,3S)-1-acetoxy-3-[2-(5-benzyloxypyridyl)]-3-tert-butyldimethylsilyloxy-2-methyl-3-propanol 
• 909913-45-7 (2S,3S)-3-[2-(5-benzyloxypyridyl)]-3-tert-butyldimethylsilyloxy-2-methyl-1-propanol 
• 909913-43-5 (2R,3S)-3-[2-(5-benzyloxypyridyl)]-3-tert-butyldimethylsilyloxy-2-methylpropanal 
• 909913-41-3 (2S,3S)-1-acetoxy-3-[2-(5-benzyloxypyridyl)]-2-methyl-3-propanol 
• 909913-46-8 (2S,3S,4S)-4-[2-(5-benzyloxypyridyl)]-2-hydroxy-3-methyl-butano-4-lactone 
• 909913-39-9 (2S,3S)-3-[2-(5-benzyloxypyridyl)]-2-methyl-1,3-propanediol 
• 909913-22-0 3-(5-benzyloxy-pyridin-2-yl)-2-methyl-3-oxo-propionic acid methyl ester 
• 909913-48-0 (2S,3S,4S)-2-azido-4-[2-(5-benzyloxypyridyl)]-3-methyl-butano-4-lactone 

Relevant articles and documents

First chiral synthesis of the N-terminal amino acid congener of nikkomycin Z based on lipase-catalyzed enantioselective acetylation of a primary alcohol possessing two stereogenic centers

A stereoselective synthesis of a versatile chiral synthon possessing two stereogenic centers, (2S,3S)-3-[2-(5-benzyloxypyridyl)]-2-methyl-1,3-propane diol 12 (>99% ee), was achieved by using a chemo-enzymatic method. The conversion of (2S,3S)-12 to the ho