Norpipanone

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Norpipanone
Clinical data
Other namesHerchst 10495, NIH-7557
ATC code
  • None
Legal status
Legal status
Identifiers
  • 4,4-diphenyl-6-(1-piperidinyl)-3-hexanone
JSmol)
  • O=C(C(c1ccccc1)(c2ccccc2)CCN3CCCCC3)CC
  • InChI=1S/C23H29NO/c1-2-22(25)23(20-12-6-3-7-13-20,21-14-8-4-9-15-21)16-19-24-17-10-5-11-18-24/h3-4,6-9,12-15H,2,5,10-11,16-19H2,1H3
  • Key:WCDSHELZWCOTMI-UHFFFAOYSA-N

Norpipanone (

international control but upon observation of case reports of addiction it was reviewed and shortly thereafter became a controlled substance.[2][3]
In the United States, it is a Schedule I controlled substance (ACSCN 9636, zero annual manufacturing quota as of 2014). The salts in use are the hydrobromide (free base conversion ratio 0.806) and hydrochloride (0.902).

Synthesis

Norpipanone synthesis:[4][5]

See also

References

  1. ^ Anvisa (2023-03-31). "RDC Nº 784 - Listas de Substâncias Entorpecentes, Psicotrópicas, Precursoras e Outras sob Controle Especial" [Collegiate Board Resolution No. 784 - Lists of Narcotic, Psychotropic, Precursor, and Other Substances under Special Control] (in Brazilian Portuguese). Diário Oficial da União (published 2023-04-04). Archived from the original on 2023-08-03. Retrieved 2023-08-16.
  2. ^
    ISBN 978-0-412-54090-5
    . Retrieved 11 May 2012.
  3. ^
    ISBN 978-0-16-050885-1
    . Retrieved 11 May 2012.
  4. doi:10.1039/JR9490000500
    .
  5. doi:10.1002/jlac.19495610107
    .


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