| Weight | 223.316 g/mol |
|---|---|
| Formula | C13H21NO2 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 5 |
2,5-Dimethoxy-4-ethylamphetamine (22004-32-6)
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- Stereospecific Actions of DOET (2,5-Dimethoxy-4-Ethylamphetamine) in Man (Archives of General Psychiatry, 1974)
- DOET(2,5-Dimethoxy-4-Ethylamphetamine), a New Psychotropic Drug: Effects of Varying Doses in Man (Archives of General Psychiatry, 1971)
- The effects of 2,5-dimethoxy-4-methylamphetamine (DOM), 2,5-dimethoxy-4-ethylamphetamine (DOET), d-amphetamine, and cocaine in rats trained with mescaline as a discriminative stimulus (Psychopharmacology, 1975)
- Altered free associations: Some cognitive effects of DOET (2, 5dimethoxy4ethylamphetamine) (Systems Research and Behavioral Science, 1970)
- Optical purity determination, conformer populations and 1H NMR spectral simplification with lanthanide shift reagents Part IX. A method for improved analytical precision for DOEt, 2,5-dimethoxy-4-ethylamphetamine (Journal of Pharmaceutical and Biomedical Analysis, 1987)
- Some pharmacological actions of 2,5dimethoxy4ethylamphetamine (DOET) in rats and mice (Journal of Pharmacy and Pharmacology, 1975)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCCC1=CC(=C(C=C1OC)CC(C)N)OC
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InChIKeyHXJKWPGVENNMCC-UHFFFAOYSA-N
- Pubchem - 2,5-Dimethoxy-4-ethylamphetamine
- Wikipedia - 4-ethyl-2,5-dimethoxyamphetamine
2,5-Dimethoxy-4-ethylamphetamine (DOET, DOE, Hecate) is a psychedelic drug of the phenethylamine and amphetamine chemical classes. It was first synthesized by Alexander Shulgin, and was described in his book PiHKAL (Phenethylamines i Have Known And Loved).
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