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| R(-)-DOI HYDROCHLORIDE POTENT AND SELECT IVE Basic information |
Product Name: | R(-)-DOI HYDROCHLORIDE POTENT AND SELECT IVE | Synonyms: | R(-)-DOI HYDROCHLORIDE POTENT AND SELECT IVE;(R)-(-)-2,5-dimethoxy-4-iodoamphetamine hydrochloride;(-)-2,5-Dimethoxy-4-iodoamphetamine hydrochloride, (-)-1-(2,5-Dimethoxy-4-iodophenyl)-2-aminopropane hydrochloride;(-)-2,5-Dimethoxy-4-iodoamphetamine hydrochloride
(R)(-)-DOI hydrochloride;(-)-1-(2,5-Dimethoxy-4-iodophenyl)-2-aminopropane Hydrochloride;(-)-2,5-Dimethoxy-4-iodoamphetamine hydrochloride | CAS: | 82864-02-6 | MF: | C11H16INO2HCl | MW: | 357.62 | EINECS: | | Product Categories: | | Mol File: | 82864-02-6.mol | |
| R(-)-DOI HYDROCHLORIDE POTENT AND SELECT IVE Chemical Properties |
Melting point | 232 °C(Solv: isopropanol (67-63-0)) | solubility | H2O: ≥20mg/mL | form | solid | color | white | optical activity | [α]22/D 12.36°, c = 2 in H2O(lit.) |
RIDADR | 2811 | WGK Germany | 3 | HazardClass | 6.1(b) | PackingGroup | III |
| R(-)-DOI HYDROCHLORIDE POTENT AND SELECT IVE Usage And Synthesis |
Uses | (-)-1-(2,5-Dimethoxy-4-iodophenyl)-2-aminopropaneHydrochloride is a useful reagent in the stereospecific synthesis of amphetamines via multi-step reactions involving corresponding aryl propanol. | Biochem/physiol Actions | Potent and selective 5-HT2 serotonin receptor agonist that crosses the blood-brain barrier; more potent enantiomer of ±-DOI hydrochloride. |
| R(-)-DOI HYDROCHLORIDE POTENT AND SELECT IVE Preparation Products And Raw materials |
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