| Identification | Back Directory | [Name]
R(-)-DOI HYDROCHLORIDE POTENT AND SELECT IVE | [CAS]
82864-02-6 | [Synonyms]
R(-)-DOI HYDROCHLORIDE POTENT AND SELECT IVE (-)-2,5-Dimethoxy-4-iodoamphetamine hydrochloride (R)-(-)-2,5-dimethoxy-4-iodoamphetamine hydrochloride (-)-1-(2,5-Dimethoxy-4-iodophenyl)-2-aminopropane Hydrochloride (-)-2,5-Dimethoxy-4-iodoamphetamine hydrochloride
(R)(-)-DOI hydrochloride (-)-2,5-Dimethoxy-4-iodoamphetamine hydrochloride, (-)-1-(2,5-Dimethoxy-4-iodophenyl)-2-aminopropane hydrochloride | [Molecular Formula]
C11H16INO2HCl | [MDL Number]
MFCD00153796 | [MOL File]
82864-02-6.mol | [Molecular Weight]
357.62 |
| Chemical Properties | Back Directory | [Melting point ]
232 °C(Solv: isopropanol (67-63-0)) | [solubility ]
H2O: ≥20mg/mL | [form ]
solid | [color ]
white | [Optical Rotation]
[α]22/D 12.36°, c = 2 in H2O(lit.) | [Water Solubility ]
H2O: ≥20mg/mL ethanol: soluble |
| Hazard Information | Back Directory | [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. |
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