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  1. World Encyclopedia
  2. Indapyrophenidone - Wikipedia
Indapyrophenidone - Wikipedia
From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Indapyrophenidone
Legal status
Legal status
  • DE: NpSG (Industrial and scientific use only)
  • UK: Under Psychoactive Substances Act
Identifiers
IUPAC name
  • 1-(2,3-dihydro-1H-inden-5-yl)-2-phenyl-2-(pyrrolidin-1-yl)-ethanone
CAS Number
  • 2055940-97-9
PubChem CID
  • 129844581
ChemSpider
  • 58858896
UNII
  • M2S46BF87V
CompTox Dashboard (EPA)
  • DTXSID601016266 Edit this at Wikidata
Chemical and physical data
FormulaC21H23NO
Molar mass305.421 g·mol−1
3D model (JSmol)
  • Interactive image
SMILES
  • O=C(C(N1CCCC1)c2ccccc2)c3ccc4CCCc4c3
InChI
  • InChI=1S/C21H23NO/c23-21(19-12-11-16-9-6-10-18(16)15-19)20(22-13-4-5-14-22)17-7-2-1-3-8-17/h1-3,7-8,11-12,15,20H,4-6,9-10,13-14H2
  • Key:JFDZZTSFBTYYDF-UHFFFAOYSA-N

Indapyrophenidone is a synthetic drug of the cathinone class that has been sold online as a designer drug.[1][2][3]

The substance is the indanyl-α-phenyl analogue of the stimulant drug α-PVP; however, it is also structurally related to diarylethylamines such as fluorolintane and UWA-001. Its mechanism of action is unknown.

See also

[edit]
  • 3,4-Pr-PipVP
  • 5-BPDi
  • Alpha-D2PV
  • βk-Ephenidine
  • Diphenidine
  • Ephenidine
  • Lefetamine
  • Methoxphenidine
  • Pyrovalerone
  • TH-PVP

References

[edit]
  1. ^ Bijlsma L, Miserez B, Ibáñez M, Vicent C, Guillamón E, Ramsey J, Hernández F (January 2016). "Identification and characterization of a novel cathinone derivative 1-(2,3-dihydro-1H-inden-5-yl)-2-phenyl-2-(pyrrolidin-1-yl)-ethanone seized by customs in Jersey". Forensic Toxicology. 34 (1): 144–150. doi:10.1007/s11419-015-0299-0. hdl:10234/146446. S2CID 2298658.
  2. ^ "1-(2,3-Dihydro-1H-inden-5-yl)-2-phenyl-2-(pyrrolidinyl-1-yl)ethan-1-one". New Synthetic Drugs Database. Archived from the original on 20 September 2018.
  3. ^ "Hírlevél" (PDF) (in Hungarian). Drog Fókuszpont. 2015. Archived (PDF) from the original on 2015-03-22. Retrieved 2016-01-27.
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