2C-AL

Chemical structure of 2C-AL

2C-AL is a psychedelic phenethylamine of the 2C family. It is known for its psychoactive effects and is structurally related to other compounds in the 2C series, such as 2C-B and 2C-I.

Chemical Structure

2C-AL is a derivative of the phenethylamine class, characterized by the presence of a methoxy group at the 2 and 5 positions of the benzene ring, and an allyl group at the 4 position. This structural modification is responsible for its unique pharmacological properties.

Pharmacology

2C-AL acts primarily as a serotonin receptor agonist, particularly at the 5-HT2A receptor, which is believed to be responsible for its psychedelic effects. The compound's interaction with these receptors leads to alterations in perception, mood, and cognition.

Effects

The effects of 2C-AL are similar to those of other 2C compounds, including visual and auditory hallucinations, altered sense of time, and changes in emotional states. The intensity and duration of these effects can vary depending on the dose and individual sensitivity.

Synthesis

The synthesis of 2C-AL involves the alkylation of 2,5-dimethoxyphenethylamine with allyl bromide. This process requires careful control of reaction conditions to ensure the correct substitution pattern on the aromatic ring.

Legal Status

The legal status of 2C-AL varies by country. In some jurisdictions, it is classified as a controlled substance due to its psychoactive properties, while in others it may be unscheduled.

Related Pages

• 2C-B
• 2C-I
• Phenethylamine
• Psychedelic drug