1572246-83-3

Basic information

• Product Name: (S)-N-[3-(2-methyl-N-tosyl-5-hexenylamino)propyl]-4-pentenamide
• Synonyms: (S)-N-[3-(2-methyl-N-tosyl-5-hexenylamino)propyl]-4-pentenamide
• CAS NO: 1572246-83-3
• Molecular Weight: 406.59
• Mol File: 1572246-83-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (S)-N-[3-(2-methyl-N-tosyl-5-hexenylamino)propyl]-4-pentenamide(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-N-[3-(2-methyl-N-tosyl-5-hexenylamino)propyl]-4-pentenamide(1572246-83-3)
• EPA Substance Registry System: (S)-N-[3-(2-methyl-N-tosyl-5-hexenylamino)propyl]-4-pentenamide(1572246-83-3)

Safety Data

• Hazardous Substances Data: 1572246-83-3(Hazardous Substances Data)

Upstream product

• 1572246-76-4 C₂₄H₂₈N₂O₅S 
• 98-59-9 p-toluenesulfonyl chloride 
• 208242-16-4 (S)-5-Amino-4-methyl-pentan-1-ol 
• 1572246-78-6 (S)-2-methyl-N-[3-(phthalimido)propyl]-N-tosyl-5-hexenamine 
• 1572246-74-2 (S)-4-methyl-5-{N-[3-(phthalimido)propyl]-N-tosylamino}-1-pentanol 
• 1572246-72-0 (S)-5-[(tert-butyldimethylsilyl)oxy]-2-methyl-N-[3-(phthalimido)propyl]-N-tosylpentanamine 
• 1572246-69-5 (S)-5-[(tert-butyldimethylsilyl)oxy]-2-methyl-N-tosylpentanamine 
• 1572245-70-5 (3R,8S,8aR)-8-methyl-5-oxo-3-phenyl-2,3,6,7,8,8a-hexahydro-5H-oxazolo[3,2-a]pyridine 
• 1572246-44-6 (S)-4-methyl-5-[(p-methylbenzenesulfonyl)amino]-1-pentanol 
• 1572246-13-9 (S)-5-{[(1R)-2-hydroxy-1-phenylethyl]amino}-4-methyl-1-pentanol 
• 40630-06-6 methyl 4-formylvalerate 
• 105-32-8 1-chloro-pent-1-en-3-one 
• 1572246-82-2 C₁₇H₂₈N₂O₂S 

Downstream Products

• 1572246-85-5 C₂₀H₃₀N₂O₃S 
• 1572246-88-8 C₂₀H₃₀N₂O₃S 

Relevant articles and documents

Access to enantiopure 4-substituted 1,5-aminoalcohols from phenylglycinol-derived δ-lactams: Synthesis of Haliclona alkaloids

LiNH2BH3-promoted reductive opening of 8-substituted phenylglycinol-derived oxazolopiperidone lactams leads to enantiopure 4-substituted-5-aminopentanols, which are used as starting building blocks in the synthesis of the Haliclona alkaloids haliclorensin C, haliclorensin, and halitulin (formal). The starting lactams are easily accessible by a cyclocondensation reaction of (R)-phenylglycinol with racemic γ-subtituted δ-oxoesters, in a process that involves a dynamic kinetic resolution.