10159-79-2 Usage
Uses
Used in Pharmaceutical Synthesis:
OCTAHYDRO-2H-QUINOLIZIN-1-YLMETHANOL is used as a building block for the synthesis of various pharmaceuticals and organic compounds. Its unique structure allows for the creation of diverse molecules with potential therapeutic properties.
Used in Medicinal Chemistry:
Due to its structural features, OCTAHYDRO-2H-QUINOLIZIN-1-YLMETHANOL may have potential applications in medicinal chemistry. Its quinolizine ring and alcohol group can be utilized in the development of new drugs and therapeutic agents.
Used in Chemical Reactions as a Reagent:
OCTAHYDRO-2H-QUINOLIZIN-1-YLMETHANOL may also be used as a reagent in chemical reactions for the creation of diverse organic molecules. Its presence in these reactions can facilitate the synthesis of a wide range of compounds with various applications across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 10159-79-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,1,5 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 10159-79:
(7*1)+(6*0)+(5*1)+(4*5)+(3*9)+(2*7)+(1*9)=82
82 % 10 = 2
So 10159-79-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H19NO/c12-8-9-4-3-7-11-6-2-1-5-10(9)11/h9-10,12H,1-8H2
10159-79-2Relevant academic research and scientific papers
Stereoselectivity in the Photoinduced Electron Transfer (PET) promoted intramolecular cyclisations of 1-alkenyl-2-silyl-piperidines and -pyrrolidines: Rapid construction of 1-azabicyclo[m.n.0] alkanes and stereoselective synthesis of (±)-isoretronecanol and (±)-epilupinine
Pandey, Ganesh,Reddy, Gottimukkula Devi,Chakrabarti, Debasish
, p. 219 - 224 (2007/10/03)
PET promoted cyclisations of 1-alkenyl-2-silyl-pyrrolidines and -piperidines 9a-d to 1-aza-bicyclo[m.n.0]alkanes have been found to be stereoselective. The five-membered ring formation gives predominantly cis products while six-membered rings are trans. Application of such cyclisations to the synthesis of (±)-isoretronecanol 22a, (±)-epilupinine 29 and related alkaloids has been demonstrated. Copyright 1996 by the Royal Society of Chemistry.
