Enallylpropymal
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| Systematic (IUPAC) name | |
|---|---|
|
(RS)-1-Methyl-5-allyl-5-isopropyl-1,3-diazinane-2,4,6-trione | |
| Identifiers | |
| CAS Number |
1861-21-8 |
| ATC code | none |
| PubChem | CID 95636 |
| ChemSpider | 86329 |
| Synonyms | Enallylpropymal |
| Chemical data | |
| Formula | C11H16N2O3 |
| Molar mass | 224.256 g/mol |
| Chirality | Racemic mixture |
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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
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