Anodyne

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Amfetaminil
Generated by the Chemistry Development Kit (http://github.com/cdk)
Molecular structure via molpic based on CDK
[]
Conformer structure via JSmol
Physical properties
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250.34 g/mol [1]
3.7 [1]
Structural Identifiers
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C17H18N2 [1]
2-phenyl-2-(1-phenylpropan-2-ylamino)acetonitrile [1]
CC(CC1=CC=CC=C1)NC(C#N)C2=CC=CC=C2 [1]
InChI=1S/C17H18N2/c1-14(12-15-8-4-2-5-9-15)19-17(13-18)16-10-6-3-7-11-16/h2-11,14,17,19H,12H2,1H3 [1]
InChIKeyNFHVTCJKAHYEQN-UHFFFAOYSA-N [1]

Amfetaminil

Amfetaminil (also known as Amphetaminil, Amfetaminilum, anfetaminilo, N-(α-Methylphenethyl)-2-phenylglycinonitrile, 241-560-8, Aponeuron, AN 1, ((α-Methylphenethyl)amino)phenylacetonitrile, Acetonitrile, ((α-methylphenethyl)amino)phenyl- or Acetonitrile, [(α-methylphenethyl)amino]phenyl-) is a substance of the amphetamine class.

Chemistry

 []

Amfetaminil is a racemic mixture of the

Stereoisomers
(1R,10S)-AmfetaminilGenerated by the Chemistry Development Kit (http://github.com/cdk)
(1S,10S)-AmfetaminilGenerated by the Chemistry Development Kit (http://github.com/cdk)
(1R,10R)-AmfetaminilGenerated by the Chemistry Development Kit (http://github.com/cdk)
(1S,10R)-AmfetaminilGenerated by the Chemistry Development Kit (http://github.com/cdk)

Pharmacology

Amfetaminil acts as a for:

Active metabolites
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Amphetamine Generated by the Chemistry Development Kit (http://github.com/cdk)

See also []

  • Substituted amphetamines
  • Anodyne

    • External links []

    References []

    1. National Center for Biotechnology Information. PubChem Compound Summary for CID 28615, Amfetaminil. Accessed July 19, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/28615

    2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Amfetaminil. UNII: 0XU0V77JVE. Global Substance Registration System. Accessed July 19, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/0XU0V77JVE