Anodyne

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Amphecloral
Generated by the Chemistry Development Kit (http://github.com/cdk)
Molecular structure via molpic based on CDK
Physical properties
[]
264.6 g/mol [1]
4.1 [1]
Structural Identifiers
[]
C11H12Cl3N [1]
2,2,2-trichloro-N-(1-phenylpropan-2-yl)ethanimine [1]
CC(CC1=CC=CC=C1)N=CC(Cl)(Cl)Cl [1]
InChI=1S/C11H12Cl3N/c1-9(15-8-11(12,13)14)7-10-5-3-2-4-6-10/h2-6,8-9H,7H2,1H3 [1]
InChIKeyVBZDETYCYXPOAK-UHFFFAOYSA-N [1]

Amphecloral

Amphecloral (also known as α-Methyl-N-(2,2,2-trichloroethylidene)benzeneethanamine, Amfecloral, Anfecloral, Amfecloral, (+)-, WZS9L0Z92R, 6015XOA0BI, α-Methyl-N-(2,2,2-trichloroethylidene)phenethylamine, 25394-63-2, 71528-69-3 or Amphechloral) is a prodrug and codrug substance of the amphetamine class.

Chemistry

 []

Amphecloral is a racemic mixture of the

Stereoisomers
(R)-AmphecloralGenerated by the Chemistry Development Kit (http://github.com/cdk)
(S)-AmphecloralGenerated by the Chemistry Development Kit (http://github.com/cdk)

Pharmacology

Amphecloral acts as a for:

Active metabolites
 []
Chloral hydrate Generated by the Chemistry Development Kit (http://github.com/cdk)
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 21759, Amphecloral. Accessed July 19, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/21759

    2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Amphecloral. UNII: S0DYI19OEX. Global Substance Registration System. Accessed July 19, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/S0DYI19OEX