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

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

Names
IUPAC name (RS)-2-[4-(2-Fluoro-ethyl)-2,5-dimethoxy-phenyl]-1-methyl-ethylamine
Other names 1-[4-(2-fluoroethyl)-2,5-dimethoxyphenyl]propan-2-amine
Identifiers
CAS Number	121649-01-2 N
ChEMBL	ChEMBL123685 Y
ChemSpider	21106293 Y
Jmol 3D model	Interactive image Interactive image
InChI 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 Y Key: QLENKWFQUHHBKZ-UHFFFAOYSA-N Y InChI=1/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 Key: QLENKWFQUHHBKZ-UHFFFAOYAO
SMILES C1(=CC(=C(C=C1CC(C)N)OC)CCF)OC COc1cc(CC(C)N)c(cc1CCF)OC
Properties
Chemical formula	C13H20NO2F
Molar mass	241.31 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

DOEF, or 4-fluoroethyl-2,5-methoxyamphetamine, is a lesser-known psychedelic drug and a substituted amphetamine. DOEF was first synthesized by Alexander Shulgin. In his book PiHKAL (Phenethylamines i Have Known And Loved), the dosage range is listed as 2-3.5[mg], and the duration is listed as 12–16 hours. DOEF produces increased appreciation of music, closed-eye visuals, increased sexual pleasure, and intense slowing of time. Very little data exists about the pharmacological properties, metabolism, and toxicity of DOEF.

See also

• 2,5-Dimethoxy-4-Substituted Amphetamines

External links

• DOEF Entry in PiHKAL
• DOEF Entry in PiHKAL • info