1125824-45-4

Basic information

• Product Name: [(S)-2-[(2S,6R)-1-methyl-6-(2-oxo-2-phenylethyl)piperidin-2-yl]-1-phenylethyl acetate]
• Synonyms: [(S)-2-[(2S,6R)-1-methyl-6-(2-oxo-2-phenylethyl)piperidin-2-yl]-1-phenylethyl acetate]
• CAS NO: 1125824-45-4
• Molecular Weight: 379.499
• Mol File: 1125824-45-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: [(S)-2-[(2S,6R)-1-methyl-6-(2-oxo-2-phenylethyl)piperidin-2-yl]-1-phenylethyl acetate](CAS DataBase Reference)
• NIST Chemistry Reference: [(S)-2-[(2S,6R)-1-methyl-6-(2-oxo-2-phenylethyl)piperidin-2-yl]-1-phenylethyl acetate](1125824-45-4)
• EPA Substance Registry System: [(S)-2-[(2S,6R)-1-methyl-6-(2-oxo-2-phenylethyl)piperidin-2-yl]-1-phenylethyl acetate](1125824-45-4)

Safety Data

• Hazardous Substances Data: 1125824-45-4(Hazardous Substances Data)

Upstream product

• 108-24-7 acetic anhydride 
• 90-69-7 lobeline 
• 1146626-22-3 lobelanidine monoacetate 

Downstream Products

• 90-69-7 lobeline 

Relevant articles and documents

Elucidating absolute configuration of unsaturated alcohols via enantioselective acylation reactions

Enantioselective nucleophilic acylation catalysis provides a simple method of determining absolute configuration for unsaturated alcohols. Extension of this technique to natural products and synthetic compounds, as well as current limitations of this appr

Indirect trapping of the retroconjugate addition reaction intermediate involved in the epimerization of lobeline: Application to the synthesis of (-)-sedamine

Alkyl chloroformates induced indirect trapping of the retroconjugate addition reaction intermediate involved in the epimerization of lobeline is described. This strategy was applied to the conversion of (-)-lobeline to (-)-sedamine in high overall yield.