1352966-47-2

Basic information

• Product Name: (E)-1-((2S,6S)-1-benzyl-6-methylpiperidin-2-yl)hept-1-en-3-one
• Synonyms: (E)-1-((2S,6S)-1-benzyl-6-methylpiperidin-2-yl)hept-1-en-3-one
• CAS NO: 1352966-47-2
• Molecular Weight: 299.456
• Mol File: 1352966-47-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (E)-1-((2S,6S)-1-benzyl-6-methylpiperidin-2-yl)hept-1-en-3-one(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-1-((2S,6S)-1-benzyl-6-methylpiperidin-2-yl)hept-1-en-3-one(1352966-47-2)
• EPA Substance Registry System: (E)-1-((2S,6S)-1-benzyl-6-methylpiperidin-2-yl)hept-1-en-3-one(1352966-47-2)

Safety Data

• Hazardous Substances Data: 1352966-47-2(Hazardous Substances Data)

Upstream product

• 61728-15-2 2-oxohexylphosphonic acid dimethyl ester 
• 1352966-44-9 ((2S,6S)-1-benzyl-6-methylpiperidin-2-yl)methanol 
• 1352966-43-8 (2S,6S)-1-benzyl-2-((tert-butyldimethylsilyloxy)methyl)-6-methylpiperidine 
• 1352966-42-7 (2S,6S)-2-((tert-butyldimethylsilyloxy)methyl)-6-methyl-piperidine 
• 1352966-41-6 (S,E)-benzyl 1-(tert-butyldimethylsilyloxy)-6-oxohept-4-en-2-ylcarbamate 

Relevant articles and documents

Synthesis of (-)-dihydropinidine, (2S,6R)-isosolenopsin and (+)-monomorine via a chiral synthon from l-aspartic acid

The use of a β-amino aldehyde derived from l-aspartic acid as a chiral synthon to construct 2,6-disubstituted piperidines is described. The synthesis of (-)-dihydropinidine·HCl, (2S,6R)-isosolenopsin·HCl and (+)-monomorine has been achieved from this chiral synthon using a Wittig reaction followed by hydrogenation (reductive cyclization) as the key steps.