Thiothinone, also known as β-ketomethiopropamine or βk-methiopropamine (βk-MPA) is a stimulant that is the β-keto-substituted analog of methiopropamine and has been sold online as a designer drug.[1][2][3] It is structurally related to methcathinone however the phenyl group has been substituted for thiophene instead.
Clinical data | |
---|---|
Other names | β-Ketomethiopropamine; βk-Methiopropamine; βk-MPA |
Legal status | |
Legal status | |
Identifiers | |
| |
CAS Number |
|
PubChem CID | |
ChemSpider | |
UNII | |
CompTox Dashboard (EPA) | |
Chemical and physical data | |
Formula | C8H11NOS |
Molar mass | 169.24 g·mol−1 |
3D model (JSmol) | |
| |
|
Thiothinone was also reported to be a pyrolysis product of methiopropamine.[4]
See also
edit- 5-Cl-bk-MPA
- α-Pyrrolidinopentiothiophenone (α-PVT)
- Methcathinone
- Methiopropamine, non-ketone counterpart
References
edit- ^ "2-Thiothinone (hydrochloride)". Cayman Chemical. Retrieved 9 September 2015.
- ^ Blicke FF, Burckhalter JS (March 1942). "α-Thienylaminoalkanes". Journal of the American Chemical Society. 64 (3): 477–480. doi:10.1021/ja01255a001.
- ^ Gambaro V, Casagni E, Dell'Acqua L, Roda G, Tamborini L, Visconti GL, Demartin F (January 2016). "Identification and characterization of a new designer drug thiothinone in seized products". Forensic Toxicology. 34 (1): 174–178. doi:10.1007/s11419-015-0289-2. S2CID 25991798.
- ^ Bouso ED, Gardner EA, O'Brien JE, Talbot B, Kavanagh PV (July–August 2014). "Characterization of the pyrolysis products of methiopropamine". Drug Testing and Analysis. 6 (7–8): 676–83. doi:10.1002/dta.1571. PMID 24166818.