157948-87-3

Basic information

• Product Name: N-Benzyl-N-(non-8-en-2-ynyl)-N-(pent-3-ynyl)amine
• Synonyms: N-Benzyl-N-(non-8-en-2-ynyl)-N-(pent-3-ynyl)amine
• CAS NO: 157948-87-3
• Molecular Weight: 293.452
• Mol File: 157948-87-3.mol

Chemical Properties

• CAS DataBase Reference: N-Benzyl-N-(non-8-en-2-ynyl)-N-(pent-3-ynyl)amine(CAS DataBase Reference)
• NIST Chemistry Reference: N-Benzyl-N-(non-8-en-2-ynyl)-N-(pent-3-ynyl)amine(157948-87-3)
• EPA Substance Registry System: N-Benzyl-N-(non-8-en-2-ynyl)-N-(pent-3-ynyl)amine(157948-87-3)

Safety Data

• Hazardous Substances Data: 157948-87-3(Hazardous Substances Data)

Upstream product

• 100-46-9 benzylamine 
• 143427-56-9 N-benzylpent-3-yn-1-amine 
• 18719-27-2 5-bromo-pent-2-yne 
• 18922-04-8 6-iodohex-1-ene 
• 165461-04-1 N-Benzyl-N-(pent-3-ynyl)-N-(prop-2-ynyl)amine 

Downstream Products

• 157948-96-4 1-Benzyl-4-((E)-ethylidene)-3-((Z)-hept-6-enylidene)piperidine 

Relevant articles and documents

Zirconocene-mediated synthesis of 3,4-disubstituted piperidines and reduced isoquinolines

Intramolecular cocyclisation of 4-azaocta-1,7-dienes, -1-en-7-ynes, -7- en-1-ynes and -1,7-diynes using 'zirconocene' equivalents affords 3-aza-8- zirconabicyclo[4.3.0]nonanes, -6-enes, -9-enes or -6,9-dienes. Protonolysis, iodinolysis, or carbonylation of these complexes affords 3,4-disubstitued piperidines. Exocyclic 1,3-dienes formed from the coupling/protonolysis of 4- azaocta-1,7-diynes react with activated dienophiles to yield reduced isoquinolines.