DOEF | |
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Molecular structure via molpic | |
Conformer structure via 3Dmol.js | |
Molecular formula | C13H20FNO2[1] |
Molecular mass | 241.30 g/mol[1] |
Predicted LogP | 2.6[1] |
Chirality | racemic[2] |
Identifiers [] | |
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IUPAC name | 1-[4-(2-fluoroethyl)-2,5-dimethoxyphenyl]propan-2-amine[1] |
SMILES | CC(CC1=C(C=C(C(=C1)OC)CCF)OC)N[1] |
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[1] |
InChIKey | QLENKWFQUHHBKZ-UHFFFAOYSA-N[1] |
Dosing |
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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
External links
- 2,5-Dimethoxy-4-(2-fluoroethyl)amphetamine (Wikipedia)
- 2,5-Dimethoxy-4-(2-fluoroethyl)amphetamine (Wikidata)
- 2,5-Dimethoxy-4-(2-fluoroethyl)amphetamine (PubChem)
- 2,5-Dimethoxy-4-(2-fluoroethyl)amphetamine (ChEMBL)
- 2,5-Dimethoxy-4-(2-fluoroethyl)amphetamine (Common Chemistry)
- 2,5-Dimethoxy-4-(2-fluoroethyl)amphetamine (UNII)
- 2,5-Dimethoxy-4-(2-fluoroethyl)amphetamine (EPA DSSTox)
References
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.
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