79297-23-7

Basic information

• Product Name: (1R,2S)-2-<(ethoxycarbonyl)amino>-1-phenyl-1-propanol
• Synonyms: (1R,2S)-2-<(ethoxycarbonyl)amino>-1-phenyl-1-propanol
• CAS NO: 79297-23-7
• Molecular Weight: 223.272
• Mol File: 79297-23-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (1R,2S)-2-<(ethoxycarbonyl)amino>-1-phenyl-1-propanol(CAS DataBase Reference)
• NIST Chemistry Reference: (1R,2S)-2-<(ethoxycarbonyl)amino>-1-phenyl-1-propanol(79297-23-7)
• EPA Substance Registry System: (1R,2S)-2-<(ethoxycarbonyl)amino>-1-phenyl-1-propanol(79297-23-7)

Safety Data

• Hazardous Substances Data: 79297-23-7(Hazardous Substances Data)

Upstream product

• 873-66-5 1-propenylbenzene 
• 118-52-5 1,3-dichloro-5,5-dimethylhydantoin 
• 51-79-6 urethane 
• 79219-15-1 (S)-2-<(ethoxycarbonyl)amino>-1-phenyl-1-propanone 

Downstream Products

• 182051-38-3 (2S,4S,5R)-2-(2'-bromoethyl)-N-ethoxycarbonyl-5-phenyl-4-methyl-1,3-oxazolidine 
• 299-42-3 ephedrine 
• 16251-45-9 (4S,5R)-4-methyl-5-phenyl-oxazolidin-2-one 
• 90-82-4 pseudoephedrine 
• 492-41-1 (1R,2S)-norephedrine 
• 492-39-7 (1S,2S)-2-amino-1-phenylpropanol 
• 301307-97-1 5(S)-methyl-4(S)-phenyl-oxazolidin-2-one 
• 29238-31-1 α--propiophenon 

Relevant articles and documents

Process for preparing β-hydroxycarbamates and their conversion to oxazolidinones

A process for preparing a β-hydroxy carbamate product is disclosed. The process comprises reacting an olefin compound containing at least one carbon-carbon double bond with a carbamate in an aqueous solvent and in the presence of a base, an osmium catalys

Erythro-Directive Reduction of α-Substituted Alkanones by Means of Hydrosilanes in Acidic Media

Hydrosilane reduced α-oxy and α-amino ketones and β-keto acid derivatives in trifluoroacetic acid to afford the corresponding erythro alcohols with high diastereoselectivity.The reaction proceeded without racemization at the carbon α to the carbonyl group.The erythro-directive reduction was explained in terms of the proton-bridged Cram cyclic model and successfully applied to the synthesis of physiologically important amino alcohols such as l-ephedrine, l-methoxamine, and erythro-2-methyl-3-piperidino-1-phenylpropanol.