1219498-04-0

Basic information

• Product Name: (S)-2-[4-hydroxynonanamide]-3-phenyl-N-[(R)-1-phenylethyl]propanamide
• Synonyms: (S)-2-[4-hydroxynonanamide]-3-phenyl-N-[(R)-1-phenylethyl]propanamide
• CAS NO: 1219498-04-0
• Molecular Weight: 424.583
• Mol File: 1219498-04-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (S)-2-[4-hydroxynonanamide]-3-phenyl-N-[(R)-1-phenylethyl]propanamide(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-2-[4-hydroxynonanamide]-3-phenyl-N-[(R)-1-phenylethyl]propanamide(1219498-04-0)
• EPA Substance Registry System: (S)-2-[4-hydroxynonanamide]-3-phenyl-N-[(R)-1-phenylethyl]propanamide(1219498-04-0)

Safety Data

• Hazardous Substances Data: 1219498-04-0(Hazardous Substances Data)

Upstream product

• 104-61-0 γ-nonalactone 
• 133287-30-6 (S)-2-amino-3-phenyl-N-[(R)-1-phenylethyl]propanamide 

Relevant articles and documents

Synthesis of optically active γ-valerolactone and γ-nonanolactone via optical resolution using chiral amine derived from amino acid

Optically active γ-valerolactone and γ-nonanolactone have been synthesized via optical resolution using a newly developed chiral amine derived from L-phenylalanine. Both racemic γ-lactones were transformed to corresponding diastereomeric amides by amidation with the optical resolution agent. Fractional crystallization of diastereomeric amides, recrystallization of each diastereomer, and subsequent hydrolysis gave optically active γ-valerolactone and γ-nonanolactone with sufficient enantiomeric excess and isolated yield. The optical resolution agent was recovered after hydrolysis.