Anodyne

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α-D2PV
Generated by the Chemistry Development Kit (http://github.com/cdk)
Salts
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Molecular structure via molpic based on CDK
Physical properties
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265.3 g/mol [1]
3.9 [1]
Structural Identifiers
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C18H19NO [1]
1,2-diphenyl-2-pyrrolidin-1-ylethanone [1]
C1CCN(C1)C(C2=CC=CC=C2)C(=O)C3=CC=CC=C3 [1]
InChI=1S/C18H19NO/c20-18(16-11-5-2-6-12-16)17(19-13-7-8-14-19)15-9-3-1-4-10-15/h1-6,9-12,17H,7-8,13-14H2 [1]
InChIKeyGQCCTZGWWWUYLS-UHFFFAOYSA-N [1]

α-Pyrrolidino-2-phenylacetophenone

α-Pyrrolidino-2-phenylacetophenone (also known as α-D2Pv, 1,2-diphenyl-2-(1-pyrrolidinyl)ethanone, α-Phenyl-α-pyrrolidinoacetophenone, Ethanone, 1,2-diphenyl-2-(1-pyrrolidinyl), α-D2PV or 1,2-diphenyl-2-(pyrrolidin-1-yl)ethan-1-one) is a substance of the diarylethylamine class.

Chemistry

Salts []

α-Pyrrolidino-2-phenylacetophenone is typically found in the form of its hydrochloride salt.

 []

α-Pyrrolidino-2-phenylacetophenone is a racemic mixture of the optical stereoisomers

Stereoisomers
(+)-α-Pyrrolidino-2-phenylacetophenoneGenerated by the Chemistry Development Kit (http://github.com/cdk)
(-)-α-Pyrrolidino-2-phenylacetophenoneGenerated by the Chemistry Development Kit (http://github.com/cdk)
Anodyne Usernotes
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0xea / α-Pyrrolidino-2-phenylacetophenone[hydrochloride] via Insufflated and IntravenousCauses Significant and a rather Intoxication and Dissociating

See also []

  • Substituted diarylethylamines
  • Anodyne

    • External links []

    References []

    1. National Center for Biotechnology Information. PubChem Compound Summary for CID 33957, α-Pyrrolidino-2-phenylacetophenone. Accessed July 13, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/33957

    2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. α-Pyrrolidino-2-phenylacetophenone. UNII: 5EB3HC2KW8. Global Substance Registration System. Accessed July 13, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/5EB3HC2KW8