299210-03-0

Basic information

• Product Name: (R_S,3R,5S)-(-)-methoxy-N-methyl-3-hydroxy-5-(3,4-dimethoxyphenyl)-5-N-(p-toluenesulfinyl)pentanamide
• Synonyms: (R_S,3R,5S)-(-)-methoxy-N-methyl-3-hydroxy-5-(3,4-dimethoxyphenyl)-5-N-(p-toluenesulfinyl)pentanamide
• CAS NO: 299210-03-0
• Molecular Weight: 450.556
• Mol File: 299210-03-0.mol

Chemical Properties

• CAS DataBase Reference: (R_S,3R,5S)-(-)-methoxy-N-methyl-3-hydroxy-5-(3,4-dimethoxyphenyl)-5-N-(p-toluenesulfinyl)pentanamide(CAS DataBase Reference)
• NIST Chemistry Reference: (R_S,3R,5S)-(-)-methoxy-N-methyl-3-hydroxy-5-(3,4-dimethoxyphenyl)-5-N-(p-toluenesulfinyl)pentanamide(299210-03-0)
• EPA Substance Registry System: (R_S,3R,5S)-(-)-methoxy-N-methyl-3-hydroxy-5-(3,4-dimethoxyphenyl)-5-N-(p-toluenesulfinyl)pentanamide(299210-03-0)

Safety Data

• Hazardous Substances Data: 299210-03-0(Hazardous Substances Data)

Upstream product

• 299209-93-1 (R_S,S)-(-)-methyl-3-oxo-N-(p-toluenesulfinyl)-5-amino-5-(3,4-dimethoxyphenyl)pentanoate 
• 299209-91-9 (R)-(+)-(3,4-dimethoxybenzylidene)-p-toluenesulfinamide 
• 247089-85-6 (R)-p-toluenesulfinamide 
• 120-14-9 3,4-dimethoxy-benzaldehyde 
• 299210-11-0 (R_S,S)-(-)-methyl-N-(p-toluenesulfinyl)-3-amino-3-(3,4-dimethoxyphenyl)propanoate 
• 6638-79-5 N,O-dimethylhydroxylamine*hydrochloride 
• 299209-95-3 (R_S,3R,5S)-(-)-methyl 3-hydroxy-5-N-(p-toluenesulfinyl)amino-5-(3,4-dimethoxyphenyl)pentanoate 

Downstream Products

• 299210-05-2 (2S,4S,6S)-(-)-2-(4-benzyloxy-butyl)-6-(3,4-dimethoxy-phenyl)-piperidin-4-ol 
• 263247-25-2 (2S,4S,6S)-(-)-2-(3,4-dimethoxyphenyl)-6-(4-hydroxybutyl)-piperidin-4-ol 
• 68681-73-2 (-)-(2S,4S,9aS)-2-hydroxy-4-(3,4-dimethoxyphenyl)-decahydroquinolizidine 
• 620158-88-5 (R_S,3R,5S)-(-)-1-(3,4-dimethoxyphenyl)-1-(N-p-toluenesulfinyl)amino-3-hydroxy-5-oxo-9-chlorononane 

Relevant articles and documents

Alkaloid synthesis using chiral δ-amino β-ketoesters: A stereoselective synthesis of (-)-lasubine II

(equation presented) A highly stereoselective asymmetric synthesis of the quinolizidine alkaloid (-)-lasubine II from a δ-amino β-hydroxy ketone, a new polyfunctionalized chiral building block, is described.