1,2-Diphenylethylamine
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| Names | |
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| Preferred IUPAC name
1,2-Diphenylethan-1-amine | |
| Identifiers | |
3D model (JSmol) |
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| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.042.828 Edit this at Wikidata |
| EC Number |
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PubChem CID |
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CompTox Dashboard (EPA) |
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| Properties | |
| C14H15N | |
| Molar mass | 197.281g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25°C [77°F], 100kPa).
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Chemical compound
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 ]- ↑ 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) - ↑ 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.
- ↑ 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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