A series of 2,5-<wbr></wbr>dimethoxy phenethylamines, collectively referred to as 2Cs, have psychoactive effects. The most effective 2C compounds are substituted at the 4 position of the aromatic ring. Many are scheduled as illegal substances. 2C-<wbr></wbr>T (hydrochloride) is described formally as 2,5-<wbr></wbr>dimethoxy-<wbr></wbr>4-<wbr></wbr>methylthiophenylethylamine hydrochloride. It has structural and pharmacokinetic properties similar to the drugs mescaline (hydrochloride) (Item No. <span class=/itemid/>11950</span>) and 2C-<wbr></wbr>T-<wbr></wbr>2 (hydrochloride) (Item No. <span class=/itemid/>11891</span>). This product is intended for forensic and research purposes.
| Catalog Number | R064571 |
| CAS Number | 61638-10-6 |
| Synonyms | 2,5-Dimethoxy-4-methylthiophenethylamine |
| Molecular Formula | C11H18ClNO2S |
| Purity | 95% |
| Storage | -20°C |
| IUPAC Name | 2-(2,5-dimethoxy-4-methylsulfanylphenyl)ethanamine;hydrochloride |
| InChI | InChI=1S/C11H17NO2S.ClH/c1-13-9-7-11(15-3)10(14-2)6-8(9)4-5-12;/h6-7H,4-5,12H2,1-3H3;1H |
| InChIKey | LMLQBDIAGNIIJG-UHFFFAOYSA-N |
| SMILES | COC1=CC(=C(C=C1CCN)OC)SC.Cl |
| Reference | 1.Bruno, R.,Matthews, A.J.,Dunn, M., et al. Emerging psychoactive substance use among regular ecstasy users in Australia. Drug and Alcohol Dependence 124(1-2), 19-25 (2012). |
