| Identification | Back Directory | [Name]
1-(4-IODO-2,5-DIMETHOXYPHENYL)PROPAN-2-AMINE | [CAS]
64584-34-5 | [Synonyms]
AURORA KA-7672
4-Iodo-2,5-dieMthoxyaMphetaMine
2,5-DiMethoxy-4-iodoMethaMphetaMine
4-iodo-2,5-dimethoxyphenylisopropylamine
1-(4-IODO-2,5-DIMETHOXYPHENYL)PROPAN-2-AMINE
4-Iodo-2,5-diMethoxy-α-MethylbenzeneethanaMine
4-iodo-3-methoxy-N-(1-methoxypropan-2-yl)aniline
Benzeneethanamine, 4-iodo-2,5-dimethoxy-α-methyl-
2-(4-iodo-2,5-dimethoxyphenyl)-1-methylethylamine
4-Iodo-2,5-dimethoxyphenylisopropylamine hydrochloride, (R)-isomer
4-Iodo-2,5-dimethoxyphenylisopropylamine hydrochloride, (+-)-isomer | [Molecular Formula]
C11H16INO2 | [MDL Number]
MFCD05662244 | [MOL File]
64584-34-5.mol | [Molecular Weight]
321.15 |
| Hazard Information | Back Directory | [Uses]
2,5-Dimethoxy-4-iodoamphetamine (DOI) is a psychedelic drug and a substituted amphetamine of the phenethylamine family. It is also a powerful anti-inflammatory that is effective at doses on the order of 100 micrograms in humans, far below its effective dose as a psychedelic. Despite being a substituted amphetamine, it is not a stimulant. DOI has a stereocenter and R-(-)-DOI is the more active stereoisomer. DOI is a 5-HT2A, 5-HT2B, and 5-HT2C receptor partial agonist. Its psychedelic effects are mediated by its agonistic properties at the 5-HT2A receptor.
This is a controlled substance. | [Definition]
ChEBI: An organoiodine compound that is amphetamine bearing two methoxy substituents at positions 2 and 5 as well as an iodo substituent at position 4. |
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