Anodyne

DOEF
2,5-Dimethoxy-4-(2-fluoroethyl)amphetamine
Molecular structure via molpic
Conformer structure via 3Dmol.js
Molecular formulaC13H20FNO2[1]
Molecular mass241.30 g/mol[1]
Predicted LogP2.6[1]
Chiralityracemic[2]
Identifiers
[]
IUPAC name1-[4-(2-fluoroethyl)-2,5-dimethoxyphenyl]propan-2-amine[1]
SMILESCC(CC1=C(C=C(C(=C1)OC)CCF)OC)N[1]
InChIInChI=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[1]
InChIKeyQLENKWFQUHHBKZ-UHFFFAOYSA-N[1]
Dosing

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

2,5-Dimethoxy-4-(2-fluoroethyl)amphetamine (also known as 4-(2-Fluoroethyl)-2,5-dimethoxy-α-methylbenzeneethanamine, Benzeneethanamine, 4-(2-fluoroethyl)-2,5-dimethoxy-α-methyl-, (+-)-, Doef, Benzeneethanamine, 4-(2-fluoroethyl)-2,5-dimethoxy-α-methyl- or 1-[4-(2-Fluoroethyl)-2,5-dimethoxyphenyl]-2-propanamine) is a substance of the 2,5-dimethoxyphenethylamine class.

Chemistry

Stereochemistry

(RS)-2,5-Dimethoxy-4-(2-fluoroethyl)amphetamine is a racemic mixture of the optical stereoisomers

See also

References

  1. National Center for Biotechnology Information. PubChem Compound Summary for CID 14201982, 2,5-Dimethoxy-4-(2-fluoroethyl)amphetamine. Accessed June 17, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/14201982.

  2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. 2,5-Dimethoxy-4-(2-fluoroethyl)amphetamine. UNII: 72UT55MXE3. Global Substance Registration System. Accessed June 17, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/72UT55MXE3