For research use only. Not for therapeutic Use.
2,5-<wbr></wbr>Dimethoxyamphetamine (2,5-<wbr></wbr>DMA) (Item No. <span class=/itemid/>9001314</span>) and its 4-<wbr></wbr>substituted analogs are designer drugs which activate the serotonin 5-<wbr></wbr>HT<sub>2</sub> receptors. 4-<wbr></wbr>chloro-<wbr></wbr>2,5-<wbr></wbr>Dimethoxyamphetamine (4-<wbr></wbr>chloro-<wbr></wbr>2,5-<wbr></wbr>DMA) is an analog of 2,5-<wbr></wbr>DMA which can be found on the illicit drug market. Its physiological and toxicological properties are poorly understood. This product is intended for research and forensic applications.
| CAS Number | 42203-77-0 |
| Synonyms | 4-chloro-2,5-Dimethoxyamphetamine;DOC |
| Molecular Formula | C11H17Cl2NO2 |
| Purity | ≥95% |
| Storage | -20°C |
| IUPAC Name | 1-(4-chloro-2,5-dimethoxyphenyl)propan-2-amine;hydrochloride |
| InChI | InChI=1S/C11H16ClNO2.ClH/c1-7(13)4-8-5-11(15-3)9(12)6-10(8)14-2;/h5-7H,4,13H2,1-3H3;1H |
| InChIKey | UOWCUOAJVCUYGV-UHFFFAOYSA-N |
| SMILES | CC(CC1=CC(=C(C=C1OC)Cl)OC)N.Cl |
| Reference | 1.Chambers, J.J.,Kurrasch-Orbaugh, D.M.,Parker, M.A., et al. Enantiospecific synthesis and pharmacological evaluation of a series of super-potent, conformationally restricted 5-HT2A/2C receptor agonists. Journal of Medicinal Chemistry 44, 1003-1010 (2001) |
