Phenylethylpyrrolidine
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From Wikipedia, the free encyclopedia
Names | |
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Preferred IUPAC name
1-(2-Phenylethyl)pyrrolidine | |
Identifiers | |
3D model (JSmol)
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ChemSpider | |
PubChem CID
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CompTox Dashboard (EPA)
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Properties | |
C12H17N | |
Molar mass | 175.275 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Chemical compound
1-(2-Phenylethyl)pyrrolidine (PEP) is a chemical compound. It is an analogue of 2-phenylethylamine where the amine has been replaced by a pyrrolidine ring. The β-keto derivative is phenacylpyrrolidine and the α-methyl and β-keto (i.e., cathinone) derivative is α-pyrrolidinopropiophenone (α-PPP).
PEP is the base chemical structure for a series of stimulant drugs, including:
All of these compounds differ from PEP in that the alpha carbon is extended and a ketone is attached to the beta carbon (with the exception of prolintane), among other modifications.
See also
[edit]References
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