161806-09-3

Basic information

• Product Name: (2R,3S)-3-Acetoxy-2-bromo-N-<(4-methoxyphenyl)methyl>-N-<2,2-bis(phenylthio)ethenyl>butanamide
• Synonyms: (2R,3S)-3-Acetoxy-2-bromo-N-<(4-methoxyphenyl)methyl>-N-<2,2-bis(phenylthio)ethenyl>butanamide
• CAS NO: 161806-09-3
• Molecular Weight: 586.571
• Mol File: 161806-09-3.mol

Chemical Properties

• CAS DataBase Reference: (2R,3S)-3-Acetoxy-2-bromo-N-<(4-methoxyphenyl)methyl>-N-<2,2-bis(phenylthio)ethenyl>butanamide(CAS DataBase Reference)
• NIST Chemistry Reference: (2R,3S)-3-Acetoxy-2-bromo-N-<(4-methoxyphenyl)methyl>-N-<2,2-bis(phenylthio)ethenyl>butanamide(161806-09-3)
• EPA Substance Registry System: (2R,3S)-3-Acetoxy-2-bromo-N-<(4-methoxyphenyl)methyl>-N-<2,2-bis(phenylthio)ethenyl>butanamide(161806-09-3)

Safety Data

• Hazardous Substances Data: 161806-09-3(Hazardous Substances Data)

Upstream product

• 161906-03-2 (2R,3S)-3-acetoxy-2-bromobutyryl chloride 
• 153823-28-0 (2,2-Bis-phenylsulfanyl-vinyl)-(4-methoxy-benzyl)-amine 
• 20461-96-5 ethyl α,α-bis(phenylthio)acetate 
• 153823-24-6 Bis(phenylsulfanyl)acetaldehyde 

Relevant articles and documents

Sulfur-directed regioselective radical cyclization leading to β-lactams: Formal synthesis of (±)-PS-5 and (+)-thienamycin

A new method for the synthesis of β-lactams by tributyltin hydride (Bu3SnH)-mediated radical cyclizations of N-ethenyl-α-bromo amides bearing sulfur-substituent(s) at the terminus of the N-vinylic bond is described. N-[2-(Phenylthio)ethenyl]-α-