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DESOXY

Names
Preferred IUPAC name 2-(3,5-Dimethoxy-4-methylphenyl)ethan-1-amine
Other names 3,5-Dimethoxy-4-methylphenethylamine
Identifiers
CAS Number	63037-49-0 Y
3D model (JSmol)	Interactive image
ChEMBL	ChEMBL127679 Y
ChemSpider	21106289 Y
PubChemCID	44350128
UNII	424LJJ87HT Y
CompTox Dashboard(EPA)	DTXSID80658381
InChI InChI=1S/C11H17NO2/c1-8-10(13-2)6-9(4-5-12)7-11(8)14-3/h6-7H,4-5,12H2,1-3H3 Y Key: LLHRMWHYJGLIEV-UHFFFAOYSA-N Y InChI=1/C11H17NO2/c1-8-10(13-2)6-9(4-5-12)7-11(8)14-3/h6-7H,4-5,12H2,1-3H3 Key: LLHRMWHYJGLIEV-UHFFFAOYAV
SMILES Cc1c(cc(cc1OC)CCN)OC
Properties
Chemical formula	C11H17NO2
Molar mass	195.26 g/mol
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa). Y verify (what is YN ?) Infobox references

4-Desoxymescaline, or4-methyl-3,5-dimethoxyphenethylamine, is amescalineanalogue related to otherpsychedelicphenethylamines. It is commonly referred to asDESOXY. DESOXY was discovered byAlexander Shulgin and published in his bookPiHKAL.

The effects of DESOXY vary significantly frommescaline, despite their chemical similarity.^{[citation needed]}

A typical dosage is within the range of 40–120 mg and lasts 6–8 hours.^[1]

DESOXY acts as aserotonin5-HT₂ receptoragonist.^[2]

In 1970 theControlled Substances Act placedmescaline intoSchedule I in theUnited States. It is similarly controlled in other nations. Depending on whether or not it is intended for human consumption, 4-desoxymescaline could be considered ananalogue ofmescaline, under theFederal Analogue Act and similar bills in other countries, making it illegal to manufacture, buy, possess, or distribute without a DEA or related license.

DESOXY is also an isomer of2C-D which makes it a schedule 1 drug in the United States.

• Substituted mescaline analogue
• Biscaline

• Alexander Shulgin, Jacob, P.Structure-Activity Relationships of the Classic Hallucinogens and Their Analogs. NIDA Research Monograph 146 (Hallucinogens: An Update), 1994.

• 5-HT2A agonists
• 5-HT2B agonists
• 5-HT2C agonists
• Psychedelic phenethylamines
• Scalines

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