Allylescaline

Allylescaline

Names
IUPAC names 4-Allyloxy-3,5-dimethoxyphenethylamine 4-Allyloxy-3,5-dimethoxy-1-ethylamine
Identifiers
CAS Number	39201-75-7 N
ChEMBL	ChEMBL126803 N
ChemSpider	21106254 N
Jmol 3D model	Interactive image
InChI InChI=1S/C13H19NO3/c1-4-7-17-13-11(15-2)8-10(5-6-14)9-12(13)16-3/h4,8-9H,1,5-7,14H2,2-3H3 N Key: JNUAYHHGCXYBHX-UHFFFAOYSA-N N InChI=1/C13H19NO3/c1-4-7-17-13-11(15-2)8-10(5-6-14)9-12(13)16-3/h4,8-9H,1,5-7,14H2,2-3H3 Key: JNUAYHHGCXYBHX-UHFFFAOYAR
SMILES COc1cc(cc(OC)c1OCC=C)CCN
Properties
Chemical formula	C13H19NO3
Molar mass	237.29 g/mol
Vapor pressure	{{{value}}}
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YN ?)
Infobox references

Allylescaline, or 4-allyloxy-3,5-dimethoxyphenethylamine, is a lesser-known psychedelic drug. It is closely related in structure to mescaline. AL was first synthesized by Otakar Leminger in 1972. The compound was later synthesized by Alexander Shulgin and further described in his book PiHKAL (Phenethylamines i Have Known And Loved). The dosage range is listed as 20–35 mg, and the duration 8-12 hours. Allylescaline produces an entactogenic warmth, an entheogenic effect, and a feeling of flowing energy. Very little data exists about the pharmacological properties, metabolism, and toxicity of allylescaline.

Legal status

Allylescaline is illegal in Sweden as of 26. January 2016.

See also

• Proscaline
• Phenethylamine
• Psychedelics, dissociatives and deliriants
• Substituted phenethylamine
• Elemicin

External links

• AL Entry in PiHKAL
• AL Entry in PiHKAL • info