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1,2-Diphenylethylamine

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1,2-Diphenylethylamine
Names
IUPAC name
1,2-diphenylethanamine
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
ECHA InfoCard 100.042.828 Edit this at Wikidata
EC Number
  • 247-126-4
  • InChI=1S/C14H15N/c15-14(13-9-5-2-6-10-13)11-12-7-3-1-4-8-12/h1-10,14H,11,15H2
    Key: DTGGNTMERRTPLR-UHFFFAOYSA-N
  • C1=CC=C(C=C1)CC(C2=CC=CC=C2)N
Properties
C14H15N
Molar mass 197.281 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

1,2-Diphenylethylamine is an organic compound and the parent compound of a group of 1,2-diarylethylamine containing NMDA receptor antagonists and dissociative hallucinogens that includes diphenidine, ephenidine, fluorolintane, and methoxyphenidine among others.[1][2][3]

References

[edit]
  1. ^ Wallach J, Brandt SD (2018). "1,2-Diarylethylamine- and Ketamine-Based New Psychoactive Substances". Handbook of Experimental Pharmacology. Handbook of Experimental Pharmacology. 252: 305–352. doi:10.1007/164_2018_148. ISBN 978-3-030-10560-0. PMID 30196446.
  2. ^ Luethi D, Liechti ME (April 2020). "Designer drugs: mechanism of action and adverse effects". Archives of Toxicology. 94 (4): 1085–1133. Bibcode:2020ArTox..94.1085L. doi:10.1007/s00204-020-02693-7. PMC 7225206. PMID 32249347.
  3. ^ Katselou M, Papoutsis I, Nikolaou P, Misailidi N, Spiliopoulou C, Athanaselis S (2018). "Diphenidine: a dissociative NPS makes an entrance on the drug scene". Forensic Toxicology. 36 (2): 233–242. doi:10.1007/s11419-018-0421-1. ISSN 1860-8965. Retrieved 11 April 2025.


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