3,4-亚甲二氧基苯丙胺
- 未分配
- 澳:已禁止(S9)
- 加:Schedule I
- 德:Anlage I
- 英:Class A
- 美:附表I
- UN:Psychotropic Schedule I
- 1-(2H-1,3-Benzodioxol-5-yl)propan-2-amine
![check](http://upload.wikimedia.org/wikipedia/commons/thumb/f/fb/Yes_check.svg/7px-Yes_check.svg.png)
- 1614
- DB01509
Y
- 1555
Y
- XJZ28FJ27W
- ChEMBL6731
Y
- DTXSID40859958
![編輯維基數據鏈接](http://upload.wikimedia.org/wikipedia/commons/thumb/8/8a/OOjs_UI_icon_edit-ltr-progressive.svg/10px-OOjs_UI_icon_edit-ltr-progressive.svg.png)
- 交互式图像
- NC(C)CC1=CC2=C(C=C1)OCO2
- InChI=1S/C10H13NO2/c1-7(11)4-8-2-3-9-10(5-8)13-6-12-9/h2-3,5,7H,4,6,11H2,1H3
Y
- Key:NGBBVGZWCFBOGO-UHFFFAOYSA-N
Y
3,4-亚甲二氧基苯丙胺(英語:3,4-Methylenedioxyamphetamine,或称为:MDA)是一种兴奋剂和迷幻药物[1],分子式为C10H13NO2。
它和乙醛在氰基硼氢化钠存在下反应,可以得到N,N-二乙基-3,4-亚甲二氧基苯丙胺。[2]
参考文献
- ^ Crean RD, Davis SA, Von Huben SN, Lay CC, Katner SN, Taffe MA. Effects of (+/-)3,4-methylenedioxymethamphetamine, (+/-)3,4-methylenedioxyamphetamine and methamphetamine on temperature and activity in rhesus macaques. Neuroscience. October 2006, 142 (2): 515–525. PMC 1853374
. PMID 16876329. doi:10.1016/j.neuroscience.2006.06.033.
- ^ Ellen W. Baxter, Allen B. Reitz. John Wiley & Sons, Inc. , 编. Reductive Aminations of Carbonyl Compounds with Borohydride and Borane Reducing Agents. Hoboken, NJ, USA: John Wiley & Sons, Inc. 2002-01-09: 1–714 [2023-03-03]. ISBN 9780471264187. doi:10.1002/0471264180.or059.01. (原始内容存档于2022-03-08) (英语).