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CAS 115956-07-5

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(2a,6a,8a,9ab)-Hexahydro-8-hydroxy-2,6-methano-2H-quinolizin-3(4H)-one

Description:
(2a,6a,8a,9ab)-Hexahydro-8-hydroxy-2,6-methano-2H-quinolizin-3(4H)-one, with CAS number 115956-07-5, is a chemical compound characterized by its complex bicyclic structure, which includes a quinolizidine framework. This compound features multiple stereocenters, contributing to its potential for stereoisomerism. The presence of a hydroxyl group at the 8-position indicates that it may exhibit hydrogen bonding capabilities, influencing its solubility and reactivity. The methano bridge adds to the rigidity of the structure, which can affect its biological activity and interaction with other molecules. Typically, compounds of this class may have applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to their potential biological activities. The specific properties, such as melting point, boiling point, and solubility, would depend on the compound's purity and the conditions under which they are measured. Overall, this compound represents a unique structure that may be of interest in various chemical and biological research fields.
Formula:C10H15NO2
InChI:InChI=1/C10H15NO2/c12-9-3-7-1-6-2-8(4-9)11(7)5-10(6)13/h6-9,12H,1-5H2/t6?,7-,8+,9+
Synonyms:
  • Endo-Hexahydro-Hydroxy-2,6-Methano-2H-Quinolizin-3-(4H)-One
  • Endo-Hexahydro-8-Hydroxy-2,6-Methano-2h-Quinolizin-3(4h)-One
  • (2α,6α,8α,9αβ)-Hexahydro-8-hydroxy-2,6-methano-2H-quinoliz
  • Intermediate Of Dolasetron
  • Hexahydro-8-hydroxy-2,6-methano-2H-quinolizin(4H)-one
  • (2A,6A,8A,9Ab)-,Hexahydro-8-Hydroxy-,2,6-Methano-2H-Quinolizin-3(4H)-One(Intermediateofdolasetron)
  • (2a,6a,8a,9ab)-,hexahydro-8-hydroxy-,2,6-Methano-2H-quinolizin-3(4H)-one (intermediate of dolasetron)
  • 8-hydroxyhexahydro-2H-2,6-methanoquinolizin-3(4H)-one
  • (6R,8R,9aS)-8-hydroxyhexahydro-2H-2,6-methanoquinolizin-3(4H)-one
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