2,5-Dimethoxy-4-cyanoamphetamine
Chemical compound
2,5-Dimethoxy-4-cyanoamphetamine | |
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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.
Chemical Structure and Properties[edit | edit source]
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 C12H16NO2, and it has a molecular weight of 206.26 g/mol.
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.
Pharmacology[edit | edit source]
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.
Effects[edit | edit source]
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.
Synthesis[edit | edit source]
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.
Legal Status[edit | edit source]
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.
Related Compounds[edit | edit source]
- 2,5-Dimethoxy-4-iodoamphetamine (DOI)
- 2,5-Dimethoxy-4-bromoamphetamine (DOB)
- 2,5-Dimethoxy-4-ethylamphetamine (DOET)
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