Enallylpropymal

From Wikipedia, the free encyclopedia
Jump to: navigation, search
Enallylpropymal
Enallylpropymal.png
Systematic (IUPAC) name
(RS)-1-Methyl-5-allyl-5-isopropyl-1,3-diazinane-2,4,6-trione
Identifiers
CAS Number 1861-21-8 YesY
ATC code none
PubChem CID 95636
ChemSpider 86329
Synonyms Enallylpropymal
Chemical data
Formula C11H16N2O3
Molar mass 224.256 g/mol
Chirality Racemic mixture
  (verify)

Enallylpropymal (Narconumal) is a barbiturate derivative developed by Hoffman la Roche in the 1930s.[1] It has sedative and hypnotic effects and is considered to have a moderate abuse potential.[2]

References[edit]

  1. ^ US Patent 2072829
  2. ^ Eddy NB, Halbach H, Isbell H, Seevers MH. Drug dependence: Its significance and characteristics. Bulletin of the World Health Organisation. 1965;32:721-733.