For research use only. Not for therapeutic Use.
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>D is described formally as 2,5-<wbr></wbr>dimethoxy-<wbr></wbr>4-<wbr></wbr>methylphenethylamine. It is a weak agonist of serotonin (5-<wbr></wbr>HT<sub></sub>) receptors (pEC<sub>50</sub> = 5.09 and 4.73 for 5-<wbr></wbr>HT<sub>2A</sub> and 5-<wbr></wbr>HT<sub>2C</sub>, respectively). Its metabolism in rats has been described. LC-<wbr></wbr>MS/MS screening methods for this designer drug have been developed. This product is intended for forensic and research purposes.
Catalog Number | R010485 |
CAS Number | 25505-65-1 |
Synonyms | 2,5-Dimethoxy-4-methylbenzeneethanamine Hydrochloride; 2-(2,5-Dimethoxy-4-methylphenyl)ethylamine Hydrochloride; 4-Methyl-2,5-dimethoxyphenethylamine Hydrochloride; 2C-D;? |
Molecular Formula | C11H18ClNO2 |
Purity | ≥95% |
Storage | -20°C |
IUPAC Name | 2-(2,5-dimethoxy-4-methylphenyl)ethanamine;hydrochloride |
InChI | InChI=1S/C11H17NO2.ClH/c1-8-6-11(14-3)9(4-5-12)7-10(8)13-2;/h6-7H,4-5,12H2,1-3H3;1H |
InChIKey | UIPCUUZBUOLEMM-UHFFFAOYSA-N |
SMILES | CC1=CC(=C(C=C1OC)CCN)OC.Cl |