792174-58-4

Basic information

• Product Name: (2S,3S)-ethyl 3-amino-2-hydroxy-3-phenylpropanoate
• Synonyms: (2S,3S)-ethyl 3-amino-2-hydroxy-3-phenylpropanoate
• CAS NO: 792174-58-4
• Molecular Weight: 209.245
• Mol File: 792174-58-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (2S,3S)-ethyl 3-amino-2-hydroxy-3-phenylpropanoate(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,3S)-ethyl 3-amino-2-hydroxy-3-phenylpropanoate(792174-58-4)
• EPA Substance Registry System: (2S,3S)-ethyl 3-amino-2-hydroxy-3-phenylpropanoate(792174-58-4)

Safety Data

• Hazardous Substances Data: 792174-58-4(Hazardous Substances Data)

Upstream product

• 1595172-39-6 (2R,3R)-3-azido-3-phenyl-2-((2,2,6,6-tetramethylpiperidin-1-yl)oxy)propanal 
• 104-55-2 3-phenyl-propenal 
• 1595172-58-9 (2R,3R)-ethyl 3-azido-3-phenyl-2-((2,2,6,6-tetramethylpiperidin-1-yl)oxy)propanoate 
• 121-39-1 (2S,3R)-ethyl 3-phenyloxirane-2-carboxylate 
• 129939-61-3 (2S,3S)-3-Azido-2-hydroxy-3-phenyl ethyl propanoate 

Downstream Products

• 1432466-68-6 (2S,3S)-ethyl 3-amino-2-hydroxy-3-phenylpropanoate 

Relevant articles and documents

Metal-organocatalytic tandem azide addition/oxyamination of aldehydes for the enantioselective synthesis of β-amino α-hydroxy esters

The tandem reaction of α,β-unsaturated aldehydes with trimethylsilyl azide and 2,2,6,6-tetramethylpiperidin-1-yloxy in the presence of chiral amines and iron complexes as the catalysts in a one-pot reaction enantioselectively afforded β-azido α-oxyaminated aldehydes. Further synthetic modification of the product afforded β-amino α-hydroxy esters in good yields with good diastereo- and enantioselectivities.