221134-15-2

Basic information

• Product Name: (2S)-2--3-phenylpropyl (E)-3-pentenoate
• Synonyms: (2S)-2--3-phenylpropyl (E)-3-pentenoate
• CAS NO: 221134-15-2
• Molecular Weight: 329.439
• Mol File: 221134-15-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2S)-2--3-phenylpropyl (E)-3-pentenoate(CAS DataBase Reference)
• NIST Chemistry Reference: (2S)-2--3-phenylpropyl (E)-3-pentenoate(221134-15-2)
• EPA Substance Registry System: (2S)-2--3-phenylpropyl (E)-3-pentenoate(221134-15-2)

Safety Data

• Hazardous Substances Data: 221134-15-2(Hazardous Substances Data)

Upstream product

• 17066-20-5 3-pentenoyl chloride 
• 84773-29-5 (S)-(+)-2-(N-methylamino)-3-phenylpropanol 

Downstream Products

• 221134-33-4 N1-<(1S)-1-benzyl-2-hydroxyethyl>-N1-methyl-3-(E)-pentenamide 
• 221134-67-4 (3S,3aR,7S,7aR)-7-benzyl-1,3,6-trimethylperhydroisoxazolo<3,4-c>pyridin-5-one 
• 221134-49-2 N1-<(1S)-1-benzyl-2-oxoethyl>-N1-methyl-(E)-3-pentenamide 

Relevant articles and documents

Stereoselective synthesis of enantiomerically pure isoxazolidine-fused δ-lactams

Enantiomerically pure isoxazolidine-fused δ-lactams have been obtained by intramolecular nitrone cycloaddition starting from homochiral amido aldehydes. The stereocenter of the homochiral precursor controls the stereochemical course of the process.