1,2-Diphenylethylamine

1,2-Diphenylethylamine

Names
IUPAC name 1,2-diphenylethanamine
Identifiers
CAS Number	25611-78-3
3D model (JSmol)	Interactive image
ChEMBL	ChEMBL351811
ChemSpider	24666
ECHA InfoCard	100.042.828
EC Number	247-126-4
PubChem CID	26482
CompTox Dashboard (EPA)	DTXSID20871350
InChI 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
SMILES C1=CC=C(C=C1)CC(C2=CC=CC=C2)N
Properties
Chemical formula	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). Infobox references

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

1. Wallach J, Brandt SD (2018). "1,2-Diarylethylamine- and Ketamine-Based New Psychoactive Substances". Handbook of Experimental Pharmacology. 252: 305–352. doi:10.1007/164_2018_148. ISBN   978-3-030-10560-0. PMID   30196446.{{cite journal}}: Cite journal requires |journal= (help)
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.