Anodyne

Enable jsmol
Expand all
Toggle theme
DOEF
Generated by the Chemistry Development Kit (http://github.com/cdk)
Molecular structure via molpic based on CDK
Physical properties
[]
241.30 g/mol [1]
2.6 [1]
Structural Identifiers
[]
C13H20FNO2 [1]
1-[4-(2-fluoroethyl)-2,5-dimethoxyphenyl]propan-2-amine [1]
CC(CC1=C(C=C(C(=C1)OC)CCF)OC)N [1]
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 [1]
InChIKeyQLENKWFQUHHBKZ-UHFFFAOYSA-N [1]

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-, Q4596787 or 1-[4-(2-Fluoroethyl)-2,5-dimethoxyphenyl]-2-propanamine) is a substance of the 2,5-dimethoxyamphetamine class.

Chemistry

 []

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

Stereoisomers
(R)-2,5-Dimethoxy-4-(2-fluoroethyl)amphetamineGenerated by the Chemistry Development Kit (http://github.com/cdk)
(S)-2,5-Dimethoxy-4-(2-fluoroethyl)amphetamineGenerated by the Chemistry Development Kit (http://github.com/cdk)

See also []

  • 4-Substituted 2,5-dimethoxyamphetamines (DOx)
  • Anodyne

    • External links []

    References []

    1. National Center for Biotechnology Information. PubChem Compound Summary for CID 14201982, 2,5-Dimethoxy-4-(2-fluoroethyl)amphetamine. Accessed July 14, 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 July 14, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/72UT55MXE3