2,5-Dimethoxy-4-(2-fluoroethyl)amphetamine
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| Names | |
|---|---|
| IUPAC name
(RS)-2-[4-(2-Fluoro-ethyl)-2,5-dimethoxy-phenyl]-1-methyl-ethylamine | |
| Other names
1-[4-(2-fluoroethyl)-2,5-dimethoxyphenyl]propan-2-amine | |
| Identifiers | |
| 121649-01-2 | |
| ChEMBL | ChEMBL123685 |
| ChemSpider | 21106293 |
| Jmol interactive 3D | Image Image |
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| Properties | |
| C13H20NO2F | |
| Molar mass | 241.31 g/mol |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
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| Infobox references | |
DOEF, or 4-fluoroethyl-2,5-methoxyamphetamine, is a lesser-known psychedelic drug and a substituted amphetamine. DOEF was first synthesized by Alexander Shulgin. In his book PiHKAL (Phenethylamines i Have Known And Loved), the dosage range is listed as 2-3.5[mg], and the duration is listed as 12–16 hours. DOEF produces increased appreciation of music, closed-eye visuals, increased sexual pleasure, and intense slowing of time. Very little data exists about the pharmacological properties, metabolism, and toxicity of DOEF.
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