CHEBI:64629 - 2-(4-iodo-2,5-dimethoxyphenyl)-1-methylethylamine

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ChEBI Name 2-(4-iodo-2,5-dimethoxyphenyl)-1-methylethylamine
Definition An organoiodine compound that is amphetamine bearing two methoxy substituents at positions 2 and 5 as well as an iodo substituent at position 4.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C11H16INO2
Net Charge 0
Average Mass 321.15470
Monoisotopic Mass 321.02257
InChI InChI=1S/C11H16INO2/c1-7(13)4-8-5-11(15-3)9(12)6-10(8)14-2/h5-7H,4,13H2,1-3H3
SMILES COc1cc(CC(C)N)c(OC)cc1I
Roles Classification
Chemical Role(s): Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
Application(s): central nervous system stimulant
Any drug that enhances the activity of the central nervous system.
(via amphetamines )
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ChEBI Ontology
Outgoing 2-(4-iodo-2,5-dimethoxyphenyl)-1-methylethylamine (CHEBI:64629) has functional parent amphetamine (CHEBI:2679)
2-(4-iodo-2,5-dimethoxyphenyl)-1-methylethylamine (CHEBI:64629) is a amphetamines (CHEBI:35338)
2-(4-iodo-2,5-dimethoxyphenyl)-1-methylethylamine (CHEBI:64629) is a dimethoxybenzene (CHEBI:51681)
2-(4-iodo-2,5-dimethoxyphenyl)-1-methylethylamine (CHEBI:64629) is a organoiodine compound (CHEBI:37142)
Synonyms Sources
1-(2,5-Dimethoxy-4-iodophenyl)-2-aminopropane ChemIDplus
1-(4-Iodo-2,5-dimethoxyphenyl)-2-aminopropane ChemIDplus
2,5-Dimethoxy-4-iodoamphetamine ChemIDplus
2,5-Dimethoxy-4-iodophenylisopropylamine ChemIDplus
4-DOI ChemIDplus
4-Iodo-2,5-dimethoxyphenylisopropylamine ChemIDplus
Registry Numbers Types Sources
2727017 Reaxys Registry Number Reaxys
64584-34-5 CAS Registry Number ChemIDplus
Last Modified
17 May 2012