80220-52-6

Basic information

• Product Name: 2H-Quinolizin-1-amine, octahydro-
• CAS NO: 80220-52-6
• Molecular Formula: C9H18N2
• Molecular Weight: 154.255
• Mol File: 80220-52-6.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 2H-Quinolizin-1-amine, octahydro-(CAS DataBase Reference)
• NIST Chemistry Reference: 2H-Quinolizin-1-amine, octahydro-(80220-52-6)
• EPA Substance Registry System: 2H-Quinolizin-1-amine, octahydro-(80220-52-6)

Safety Data

• Hazardous Substances Data: 80220-52-6(Hazardous Substances Data)

Upstream product

• 885111-49-9 (1R,9aR)-1-azidohexahydro-1H-quinolizin-4(6H)-one 
• 10447-21-9 hexahydro-quinolizin-1-one 
• 80220-51-5 1-Oxo-chinolizidin-oxim 
• 1421762-23-3 (1R,9aR)-octahydro-1-(di-tert-butyloxycarbonylamino)-1H-quinolizine 
• 1421762-21-1 (1R,9aR)-2,3,4,6,9,9a-hexahydro-N,N-di(tert-butyloxycarbonyl)-1H-quinolizin-1-amine 
• 1421762-20-0 1-(di-tert-butyloxycarbonylamino)-1,2,3,4-tetrahydroquinolizinium iodide 
• 1421762-19-7 2-[(R)-1-[di(tert-butyloxycarbonyl)amino]but-3-enyl]pyridine 

Downstream Products

• 1004-90-6 (+)-1,3,4,6,7,9a-hexahydro-2H-quinolizin 
• 67092-52-8 4-Acetylamino-5-chloro-2-methoxy-N-(1R,9aR)-octahydro-quinolizin-1-yl-benzamide 
• 67092-53-9 4-Acetylamino-5-chloro-2-methoxy-N-(1R,9aS)-octahydro-quinolizin-1-yl-benzamide 
• 1004-90-6 norlupinene 
• 10447-19-5 (9aR)-(9ar)-octahydro-quinolizin-1ξ-ol 
• 67092-55-1 (1α,9aα)-4-amino-5-chloro-2-methoxy-N-(octahydro-2H-quinolizin-1-yl)benzamide 
• 67092-54-0 (1β,9aα)-4-amino-5-chloro-2-methoxy-N-(octahydro-2H-quinolizin-1-yl)benzamide 

Relevant articles and documents

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A hydrozirconation/iodination-mediated access to tetrahydroquinolizinium salts. Application to the synthesis of Lupinine and (-)-Epiquinamide

The preparation of tetrahydroquinolizinium salts, based on a hydrozirconation/iodination sequence involving 2-pyridyl alkenes, is presented. This approach was applied to the synthesis of substituted quinolizines as illustrated by the synthesis of Lupinine

Stereoflexible total synthesis of (-)-epiquinamide

Hydroxy propiolate rearrangement to conjugated diene, Sharpless asymmetric dihydroxylation and one-pot quinolizine construction have been used as key steps in the total synthesis of (-)-epiquinamide.