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2C-V
| Column 1 |
|---|
| 2C-VI; 4-Ethenyl-2,5-dimethoxyphenethylamine; 4-Vinyl-2,5-dimethoxyphenethylamine; 2,5-Dimethoxy-4-ethenylphenethylamine; 2,5-Dimethoxy-4-vinylphenethylamine |
| Oral |
| Serotonergic psychedelic; Hallucinogen |
| 5 hours |
| IUPAC name |
| 2-(4-ethenyl-2,5-dimethoxyphenyl)ethanamine |
| .mw-parser-output .plainlist ol,.mw-parser-output .plainlist ul{line-height:inherit;list-style:none;margin:0;padding:0}.mw-parser-output .plainlist ol li,.mw-parser-output .plainlist ul li{margin-bottom:0}2888537-57-1 |
| 57474284 |
| 129433732 |
| F5U9H625TA |
| DTXSID501337027 |
| C12H17NO2 |
| 207.273 g·mol−1 |
| Interactive image |
| SMILES |
| COc1cc(C=C)c(cc1CCN)OC |
| InChI |
| InChI=1S/C12H17NO2/c1-4-9-7-12(15-3)10(5-6-13)8-11(9)14-2/h4,7-8H,1,5-6,13H2,2-3H3Key:LGLJOVNOGICITR-UHFFFAOYSA-N |
2C-V, or 2C-VI, also known as 4-ethenyl-2,5-dimethoxyphenethylamine, is a recreational designer drug from the substituted phenethylamine family, with psychedelic effects. It was first synthesised by Daniel Trachsel and colleagues in 2006. It is active at a dosage of 25 mg orally with a duration of around 5 hours. It is a controlled substance in Canada under phenethylamine blanket-ban language.
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2C (psychedelics)
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2C-AL
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2C-CP
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2C-E
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2C-YN
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2C-VI (2C-V) - Isomer Design
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