| Weight | 260.131 g/mol |
|---|---|
| Formula | C10H14BrNO2 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 4 |
4-Bromo-2,5-dimethoxyphenethylamine (66142-81-2)
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- Metabolic pathways of 4-bromo-2,5-dimethoxyphenethylamine (2C-B): analysis of phase I metabolism with hepatocytes of six species including human. (Toxicology, 2005)
- In vivo metabolism of 4-bromo-2,5-dimethoxyphenethylamine (2C-B) in the rat: identification of urinary metabolites. (Journal of Analytical Toxicology, 2002)
- 4-Bromo-2,5-dimethoxyphenethylamine (2C-B) and structurally related phenylethylamines are potent 5-HT2A receptor antagonists in Xenopus laevis oocytes (British Journal of Pharmacology, 2004)
- Metabolism of the designer drug 4-bromo-2,5-dimethoxyphenethylamine (2C-B) in mice, after acute administration (Journal of Chromatography B, 2004)
- A study of the metabolism of methamphetamine and 4-bromo-2,5-dimethoxyphenethylamine (2C-B) in isolated rat hepatocytes (Forensic Science International, 2005)
- A preliminary investigation of the psychoactive agent 4-bromo-2,5-dimethoxyphenethylamine: a potential drug of abuse (Pharmacology, Biochemistry and Behavior, 1988)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCOC1=CC(=C(C=C1CCN)OC)Br
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InChIKeyYMHOBZXQZVXHBM-UHFFFAOYSA-N
- Pubchem - 4-Bromo-2,5-dimethoxyphenethylamine
- Wikipedia - 4-bromo-2,5-dimethoxyphenethylamine
2C-B or 2,5-dimethoxy-4-bromophenethylamine is a psychedelic drug of the 2C family. It was first synthesized by Alexander Shulgin in 1974. In Shulgin's book PiHKAL, the dosage range is listed as 1224mg.
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Synthesis
Reactant
+
Methyl hydroperoxide
(Dakin oxidation)
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