Anodyne

Alphenal
Generated by the Chemistry Development Kit (http://github.com/cdk)
Molecular structure via molpic based on CDK
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Conformer structure via JSmol
Physical properties
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244.25 g/mol [1]
1.7 [1]
Structural Identifiers
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C13H12N2O3 [1]
5-phenyl-5-prop-2-enyl-1,3-diazinane-2,4,6-trione [1]
C=CCC1(C(=O)NC(=O)NC1=O)C2=CC=CC=C2 [1]
InChI=1S/C13H12N2O3/c1-2-8-13(9-6-4-3-5-7-9)10(16)14-12(18)15-11(13)17/h2-7H,1,8H2,(H2,14,15,16,17,18) [1]
InChIKeyWOIGZSBYKGQJGL-UHFFFAOYSA-N [1]

Alphenal

Alphenal (also known as Phenallymal, Alpheba, Allofenyl, Alphenate, Fenallymal, Phenallymalum, Prophenal, Allophenylum, αsem or Tubergal) is a substance of the barbiturate class.

Chemistry

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Alphenal is a achiral mixture

Legal status []

  • Canada: Alphenal is a Schedule IV substance.
  • United States: Alphenal is a Controlled substances act#Schedule III|Schedule III substance.

References []

  1. National Center for Biotechnology Information. PubChem Compound Summary for CID 8274, Alphenal. Accessed July 13, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/8274

  2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Alphenal. UNII: 7T7L08Q9JI. Global Substance Registration System. Accessed July 13, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/7T7L08Q9JI