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2,5-Dimethoxy-4-(2-fluoroethyl)amphetamine

From Wikipedia, the free encyclopedia

Pharmaceutical compound
DOEF
Clinical data
Other namesDOEF; 2,5-Dimethoxy-4-(2-fluoroethyl)amphetamine; 4-(2-Fluoroethyl)-2,5-dimethoxyamphetamine
Identifiers
  • 1-[4-(2-fluoroethyl)-2,5-dimethoxyphenyl]propan-2-amine
CAS Number
PubChemCID
ChemSpider
UNII
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC13H20FNO2
Molar mass241.306 g·mol−1
3D model (JSmol)
  • C1(=CC(=C(C=C1CC(C)N)OC)CCF)OC
  • InChI=1S/C13H20FNO2/c1-9(15)6-11-8-12(16-2)10(4-5-14)7-13(11)17-3/h7-9H,4-6,15H2,1-3H3 checkY
  • Key:QLENKWFQUHHBKZ-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

2,5-Dimethoxy-4-(2-fluoroethyl)amphetamine (DOEF) is a lesser-knownpsychedelic drug and member of theDOx family.[1][2] DOEF was first synthesized byAlexander Shulgin. In his bookPiHKAL, the dosage range is listed as 2 to 3.5 mg, and the duration is listed as 12 to 16 hours.[3] Very little data exists about the pharmacological properties, metabolism, and toxicity of DOEF.

See also

[edit]

References

[edit]
  1. ^Gerdes JM, Mathis CA, Shulgin AT (1988). "Synthesis of 1-[2′,5′-dimethoxy-4′-(β-fluoroethyl) phenyl]-2-aminopropane: studies related to18F-labeled serotonin receptor ligands".Tetrahedron Letters.29 (50):6537–6539.doi:10.1016/S0040-4039(00)82391-6.
  2. ^Trachsel D (2012). "Fluorine in psychedelic phenethylamines".Drug Testing and Analysis.4 (7–8):577–590.doi:10.1002/dta.413.PMID 22374819.
  3. ^"DOEF Entry".PiHKAL.

External links

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