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<p><b>New page</b></p><div>{{Short description|Chemical compound}}<br />
{{Drugbox<br />
| verifiedfields = changed<br />
| verifiedrevid = 477318123<br />
| image = DOCN_structure.png<br />
| image_size = 200px<br />
| IUPAC_name = 1-(4-Cyanophenyl)-2,5-dimethoxypropan-2-amine<br />
| other_names = 2,5-Dimethoxy-4-cyanoamphetamine<br />
}}<br />
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'''2,5-Dimethoxy-4-cyanoamphetamine''' ('''DOCN''') is a [[psychedelic]] [[phenethylamine]] and a member of the [[amphetamine]] class of compounds. It is known for its psychoactive effects and is structurally related to other compounds in the 2,5-dimethoxy family.<br />
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==Chemical Structure and Properties==<br />
[[File:DOCN_structure.png|Structure of 2,5-Dimethoxy-4-cyanoamphetamine|thumb|right]]<br />
2,5-Dimethoxy-4-cyanoamphetamine is characterized by the presence of a [[cyano group]] at the 4-position of the phenyl ring, along with two methoxy groups at the 2 and 5 positions. The chemical formula is C<sub>12</sub>H<sub>16</sub>NO<sub>2</sub>, and it has a molecular weight of 206.26 g/mol.<br />
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The compound is a derivative of [[amphetamine]], with the addition of methoxy groups and a cyano group, which significantly alters its pharmacological properties compared to the parent compound.<br />
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==Pharmacology==<br />
DOCN acts primarily as a [[serotonin receptor]] agonist, similar to other psychedelic amphetamines. It is believed to interact with the [[5-HT2A receptor]], which is associated with the psychedelic effects of these compounds. The presence of the cyano group may influence its binding affinity and selectivity for various serotonin receptor subtypes.<br />
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==Effects==<br />
The effects of 2,5-Dimethoxy-4-cyanoamphetamine are not well-documented in scientific literature, but it is presumed to produce effects similar to other psychedelic amphetamines such as [[2,5-Dimethoxy-4-iodoamphetamine]] (DOI) and [[2,5-Dimethoxy-4-bromoamphetamine]] (DOB). These effects may include altered perception, mood changes, and visual hallucinations.<br />
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==Synthesis==<br />
The synthesis of DOCN involves the introduction of a cyano group to the 4-position of the phenyl ring in the 2,5-dimethoxyamphetamine structure. This can be achieved through various chemical reactions, including the use of cyanide sources in the presence of appropriate catalysts.<br />
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==Legal Status==<br />
The legal status of 2,5-Dimethoxy-4-cyanoamphetamine varies by country. In some jurisdictions, it may be classified as a controlled substance due to its structural similarity to other regulated psychedelic compounds.<br />
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==Related Compounds==<br />
* [[2,5-Dimethoxy-4-iodoamphetamine]] (DOI)<br />
* [[2,5-Dimethoxy-4-bromoamphetamine]] (DOB)<br />
* [[2,5-Dimethoxy-4-ethylamphetamine]] (DOET)<br />
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==See Also==<br />
* [[Psychedelic drug]]<br />
* [[Phenethylamine]]<br />
* [[Amphetamine]]<br />
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==Related Pages==<br />
* [[List of psychedelic drugs]]<br />
* [[Serotonin receptor]]<br />
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[[Category:Psychedelic phenethylamines]]<br />
[[Category:Amphetamines]]</div>Prab