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Identifiers | |
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PubChem CID | |
Chemical and physical data | |
Formula | C19H27NO |
Molar mass | 285.431 g·mol−1 |
3D model ( JSmol) | |
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3,4-Pr-PipVP is a substituted cathinone derivative with stimulant effects which has been sold as a designer drug. [1]
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Legal status | |
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Legal status |
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Identifiers | |
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Chemical and physical data | |
Formula | C17H23NO |
Molar mass | 257.377 g·mol−1 |
3D model ( JSmol) | |
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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 have been tested have proved to be 3,4-Pr-PipVP. [2]
![]() | |
Legal status | |
---|---|
Legal status | |
Identifiers | |
| |
PubChem CID | |
Chemical and physical data | |
Formula | C19H27NO |
Molar mass | 285.431 g·mol−1 |
3D model ( JSmol) | |
| |
|
3,4-Pr-PipVP is a substituted cathinone derivative with stimulant effects which has been sold as a designer drug. [1]
![]() | |
Legal status | |
---|---|
Legal status |
|
Identifiers | |
| |
Chemical and physical data | |
Formula | C17H23NO |
Molar mass | 257.377 g·mol−1 |
3D model ( JSmol) | |
| |
|
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 have been tested have proved to be 3,4-Pr-PipVP. [2]