2-Phenyl-3-aminobutane
Clinical data | |
---|---|
Other names | β-Methylamphetamine |
Identifiers | |
IUPAC name
| |
CAS Number | |
PubChem CID | |
ChemSpider | |
CompTox Dashboard (EPA) | |
Chemical and physical data | |
Formula | C10H15N |
Molar mass | 149.237 g·mol−1 |
3D model (JSmol) | |
SMILES
| |
InChI
|
2-Phenyl-3-aminobutane (also known as β-methylamphetamine) is a stimulant of the phenethylamine class that is closely related to its α-methyl analog Pentorex.[1] It was first synthesized by the German scientists Felix Haffner and Fritz Sommer in 1939 as a stimulant with milder effects, shorter duration, lower toxicity and fewer side effects compared to previously known drugs such as amphetamine.[2]
2-Phenyl-3-aminobutane is banned in some countries as a structural isomer of methamphetamine.
See also
References
- ↑ Ledgard J (2007). A Laboratory History of Narcotics. Vol. 1: Amphetamines and Derivatives. Lulu.com. p. 81. ISBN 978-0-615-15694-1.
- ↑ Haffner F, Sommer F (22 August 1944). "Patent US 2356582 A - Stimulants suitable for combating symptoms of fatigue and process for their production". Retrieved 25 July 2015.
Adrenergic receptor modulators | |||||
---|---|---|---|---|---|
α1 |
| ||||
α2 |
| ||||
β |
| ||||
|
Phenethylamines |
|
---|---|
Amphetamines |
|
Phentermines |
|
Cathinones |
|
Phenylisobutylamines | |
Phenylalkylpyrrolidines | |
Catecholamines (and close relatives) |
|
Miscellaneous |
|
This article is issued from Offline. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.