Structure via PubChem · Public domain (PubChem)
In the Vinony graph
Vinony's link graph records 1,389 inbound references to 2-fluoroamphetamine, and connects out to 2C-G, (RS)-4-hydroxyamphetamine and phenylethylpyrrolidine.
It sits within the topics 2-Fluorophenyl compounds, Chemical pages without DrugBank identifier and Designer drugs.
Vinony links it to 6 Wikipedia language editions.
Chemical data
- Formula
- C9H12FN
- Molecular weight
- 153.2 g/mol
- IUPAC name
- 1-(2-fluorophenyl)propan-2-amine
- SMILES
- CC(CC1=CC=CC=C1F)N
- InChIKey
- GDSXNLDTQFFIEU-UHFFFAOYSA-N
- XLogP
- 1.8
- Polar surface area
- 26 Ų
- H-bond donors
- 1
- H-bond acceptors
- 2
- Formal charge
- 0
via PubChem
Wikidata facts
- Subclass of
- chemical compound
- Has part
- carbon
- Mass
- 153.095
Show 3 more facts
- chemical formula
- C₉H₁₂FN
- Commons category
- 2-Fluoroamphetamine
- canonical SMILES
- CC(CC1=CC=CC=C1F)N
Sources (2)
via Wikidata · CC0
~2 min read
Encyclopedic overview
8 sectionsContents
- Pharmacology
- Toxicology
- Legal status
- United States
- China
- Finland
- See also
- References
thumb|1 gram of 2-FA
2-Fluoroamphetamine (2-FA) is a stimulant drug from the amphetamine family which has been sold as a designer drug. 2-Fluoroamphetamine differs from 3-fluoroamphetamine and 4-fluoroamphetamine in the position of the fluorine atom on the aromatic ring, making them positional isomers of one another. The replacement of a hydrogen atom with a fluorine atom in certain compounds to facilitate passage through the blood–brain barrier, as is desirable in central nervous system pharmaceutical agents, is a common practice due to the corresponding increase in lipophilicity granted by this substitution.
Excerpted from Wikipedia’s “2-fluoroamphetamine” article, available under the CC BY-SA 4.0 licence.