Anodyne| 3-FMC | |
|---|---|
 |
| Salts [] | |
|---|---|
| Flophedrone hydrochloride | |
|
| Molecular structure via molpic | |
| Conformer structure via 3Dmol.js | |
| Molecular formula | C10H12FNO[1] |
|---|---|
| Molecular mass | 181.21 g/mol[1] |
| Predicted LogP | 1.7[1] |
| Chirality | racemic[2] |
| Identifiers [] | |
|---|---|
| IUPAC name | 1-(3-fluorophenyl)-2-(methylamino)propan-1-one[1] |
| SMILES | CC(C(=O)C1=CC(=CC=C1)F)NC[1] |
| InChI | InChI=1S/C10H12FNO/c1-7(12-2)10(13)8-4-3-5-9(11)6-8/h3-7,12H,1-2H3[1] |
| InChIKey | PQIBROLLUQSNQI-UHFFFAOYSA-N[1] |
| Dosing |
|---|
Flophedrone
Flophedrone (also known as 3-Fluoromethcathinone, 3-Flephedrone, 3'-Fluoromethcathinone, 3-Fluoro-n-methylcathinone, J2.929.934j, 1-Propanone, 1-(3-fluorophenyl)-2-(methylamino)-, pqibrolluqsnqi-uhfffaoysa-n, (S)-3-fluoromethcathinone, 2-(methylamino)-1-(3-fluorophenyl)-1-propanone or Q27266683) is a stimulant substance of the cathinone class.
Chemistry
Flophedrone is typically found in the form of its hydrochloride salt.
Stereochemistry
(RS)-Flophedrone is a racemic mixture of the optical stereoisomers:
| Stereoisomers [] |
|---|
|
(+)-3-fluoromethcathinone -3-fluoromethcathinone.svg)
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Subjective effects
| Physical effects [] |
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| Cognitive effects [] |
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| 0xea / Flophedrone[hydrochloride] via Insufflated and Intravenous | Moderate Euphoria; Very Short Duration; Strongly Increased bodily temperature; Quite Unpleasant |
Legal status
- United States: Flophedrone is a Schedule I substance.
- United Kingdom: Flophedrone is a Class B substance.
- Germany: Flophedrone is a Anlage II substance.