| 词条 | 2-Phenyl-3-aminobutane |
| 释义 |
| IUPAC_name = 3-Phenylbutan-2-amine | image = 2-Phenyl-3-aminobutane.png | tradename = | pregnancy_AU = | pregnancy_US = | pregnancy_category = | legal_status = | routes_of_administration = | bioavailability = | protein_bound = | metabolism = | elimination_half-life = | excretion = | CAS_number_Ref = | CAS_number = 21906-17-2 | ATC_prefix = | ATC_suffix = | PubChem = 210912 | ChemSpiderID = 182828 | synonyms = β-Methylamphetamine | C=10 | H=15 | N=1 | melting_point = | smiles = C1(=CC=CC=C1)C(C)C(C)N | StdInChI = 1/C10H15N/c1-8(9(2)11)10-6-4-3-5-7-10/h3-9H,11H2,1-2H3 | StdInChIKey = BKRHEVJTTWAYFJ-UHFFFAOYSA-N }}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
References1. ^{{cite book | url=https://books.google.com/books?id=mGcoAgAAQBAJ&pg=PA81 | title=A Laboratory History of Narcotics, Vol. 1 Amphetamines and Derivatives | publisher=Lulu.com | author=Jared Ledgard | year=2007 | pages=81 | isbn=0615156940}} {{Stimulants}}{{Anorectics}}{{Adrenergics}}{{Phenethylamines}}{{DEFAULTSORT:Phenyl-3-aminobutane, 2-}}{{nervous-system-drug-stub}}2. ^{{cite web | url=https://www.google.com/patents/US2356582 | title=Patent US 2356582 A - Stimulants suitable for combating symptoms of fatigue and process for their production | date=22 August 1944 | accessdate=25 July 2015 | author=Felix Haffner, Fritz Sommer}} 4 : Anorectics|Norepinephrine-dopamine releasing agents|Phenethylamines|Substituted amphetamines |
| 随便看 |
|
开放百科全书收录14589846条英语、德语、日语等多语种百科知识，基本涵盖了大多数领域的百科知识，是一部内容自由、开放的电子版国际百科全书。