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4-Phenylpiperidine

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This is an old revision of this page, as edited by CheMoBot (talk | contribs) at 19:27, 5 June 2016 (Updating {{chembox}} (changes to verified and watched fields) per Chem/Drugbox validation (report errors or bugs)). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

4-Phenylpiperidine
Names
IUPAC name
4-Phenylpiperidine
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
ECHA InfoCard 100.011.130 Edit this at Wikidata
  • InChI=1S/C11H15N/c1-2-4-10(5-3-1)11-6-8-12-9-7-11/h1-5,11-12H,6-9H2 checkY
    Key: UTBULQCHEUWJNV-UHFFFAOYSA-N checkY
  • InChI=1/C11H15N/c1-2-4-10(5-3-1)11-6-8-12-9-7-11/h1-5,11-12H,6-9H2
    Key: UTBULQCHEUWJNV-UHFFFAOYAO
  • c1cc(ccc1)C2CCNCC2
  • c1ccc(cc1)C2CCNCC2
Properties
C11H15N
Molar mass 161.248 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

4-Phenylpiperidine is a chemical compound. It features a benzene ring bound to a piperidine ring.

4-Phenylpiperidine is the base structure for a variety of opioids, such as pethidine (meperidine), ketobemidone, alvimopan, loperamide, and diphenoxylate. Other pharmaceutical drugs derived from 4-phenylpiperdine include haloperidol, ropitoin, vesamicol, enefexine, and Altapizone.

A related compound is 4-benzylpiperidine, in which the rings are separated by a methylene bridge.

See also