Anodyne| Alphenal | |
|---|---|
 | |
| Molecular structure via molpic | |
| Conformer structure via 3Dmol.js | |
| Molecular formula | C13H12N2O3[1] |
| Molecular mass | 244.25 g/mol[1] |
| Predicted LogP | 1.7[1] |
| Chirality | achiral[2] |
| Identifiers [] | |
|---|---|
| IUPAC name | 5-phenyl-5-prop-2-enyl-1,3-diazinane-2,4,6-trione[1] |
| SMILES | C=CCC1(C(=O)NC(=O)NC1=O)C2=CC=CC=C2[1] |
| InChI | 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] |
| InChIKey | WOIGZSBYKGQJGL-UHFFFAOYSA-N[1] |
| Dosing |
|---|
Alphenal
Alphenal (also known as Phenallymal, Alpheba, Allofenyl, Alphenate, Fenallymal, Phenallymalum, Prophenal, Allophenylum, αsem or Tubergal) is a substance of the barbiturate class.
Chemistry
Stereochemistry
Alphenal is a achiral mixture
Legal status
- Canada: Alphenal is a Schedule IV substance.
- United States: Alphenal is a Schedule III substance.