10159-79-2 Usage
General Description
OCTAHYDRO-2H-QUINOLIZIN-1-YLMETHANOL is a chemical compound that is a derivative of quinolizine, a bicyclic organic compound. It contains a quinolizine ring with an additional alcohol group attached to the quinolizine carbon atom. OCTAHYDRO-2H-QUINOLIZIN-1-YLMETHANOL is used as a building block in the synthesis of various pharmaceuticals and organic compounds. It may also have potential applications in medicinal chemistry due to its structural features. Additionally, OCTAHYDRO-2H-QUINOLIZIN-1-YLMETHANOL may be used as a reagent in chemical reactions for the creation of diverse organic molecules.
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 articles and documents
On the knowledge of the rearrangement of lupinine and epilupinine with metallic sodium.
WINTERFELD,JAP
, p. 14 - 15 (1962)
-
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.
