3,4-Pr-PipVP

Chemical compound From Wikipedia, the free encyclopedia

3,4-Pr-PipVP is a substituted cathinone derivative with stimulant effects which has been sold as a designer drug.[1]

Legal status
FormulaC19H27NO
Molar mass285.431 g·mol−1
Quick facts Legal status, Identifiers ...
3,4-Pr-PipVP
Legal status
Legal status
Identifiers
  • 1-(2,3-dihydro-1H-inden-5-yl)-2-piperidin-1-ylpentan-1-one
PubChem CID
Chemical and physical data
FormulaC19H27NO
Molar mass285.431 g·mol−1
3D model (JSmol)
  • CCCC(C(=O)C1=CC2=C(CCC2)C=C1)N3CCCCC3
  • InChI=1S/C19H27NO/c1-2-7-18(20-12-4-3-5-13-20)19(21)17-11-10-15-8-6-9-16(15)14-17/h10-11,14,18H,2-9,12-13H2,1H3
  • Key:XCBQKBNQNYAXPN-UHFFFAOYSA-N
Close

3,4-EtPV

Quick facts Legal status, Identifiers ...
3,4-EtPV
Legal status
Legal status
  • DE: legal
Identifiers
  • 1-(bicyclo[4.2.0]octa-1,3,5-trien-3-yl)-2-(pyrrolidin-1-yl)pentan-1-one
PubChem CID
Chemical and physical data
FormulaC17H23NO
Molar mass257.377 g·mol−1
3D model (JSmol)
  • O=C(C(CCC)N1CCCC1)c1ccc2CCc2c1
  • InChI=InChI=1S/C17H23NO/c1-2-5-16(18-10-3-4-11-18)17(19)15-9-7-13-6-8-14(13)12-15/h7,9,12,16H,2-6,8,10-11H2,1H3
  • Key:GJPHTMBPBAUZGR-UHFFFAOYSA-N
Close

3,4-Pr-PipVP was marketed online since 2021 as 3,4-EtPV, which is not covered by the controlled drug analogue laws in some jurisdictions such as Germany and Holland. However, while genuine 3,4-EtPV can be made and is now available from analytical suppliers as a reference standard, the benzocyclobutene ring system is relatively unstable and the synthesis is challenging, and all samples of supposed 3,4-EtPV that were tested proved to be 3,4-Pr-PipVP,[2] until July 2024 when a genuine sample of 3,4-EtPV was finally identified in Germany.[3]

See also

References

Related Articles

Wikiwand AI