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N-甲基-2,4,5-三甲氧基安非他命

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N-甲基-2,4,5-三甲氧基安非他命
臨床資料
其他名稱METHYL-TMA-2; N-Me-TMA-2; N-Methyl-TMA-2; α,N-Dimethyl-2C-O; N-Methyl-2,4,5-trimethoxyamphetamine
识别信息
  • N-methyl-1-(2,4,5-trimethoxyphenyl)propan-2-amine
PubChem CID
化学信息
化学式C13H21NO3
摩尔质量239.32 g·mol−1
3D模型(JSmol英语JSmol
  • CC(CC1=CC(=C(C=C1OC)OC)OC)NC
  • InChI=1S/C13H21NO3/c1-9(14-2)6-10-7-12(16-4)13(17-5)8-11(10)15-3/h7-9,14H,6H2,1-5H3
  • Key:USTLBRBKMWJINX-UHFFFAOYSA-N

N-甲基-2,4,5-三甲氧基苯丙胺N-Me-TMA-2)是一种苯乙胺、苯丙胺及DOx类药物,化学式为C13H21NO3[1][2]它最早在1984年于学术文献中被报道,[2][3]并于1991年在亚历山大·舒尔金的著作《PiHKAL》中被记载。[1]

参考文献

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  1. ^ 1.0 1.1 Template:CitePiHKAL "Three additional N-methylated homologues of known psychedelics warrant mention, but do not really deserve separate recipes. This is because they have had only the most cursory assaying, which I have learned about by personal correspondence. [...] METHYL-TMA [...] had been run up in several trials to a maximum of 240 [mg], with some mental disturbances mentioned only at this highest level. METHYL-TMA-2 [...] had been tried at up to 120 [mg] without any effects. METHYL-TMA-6 [...] had been tried at up to 30 [mg] and it, too, was apparently without effects. These are reports that I have heard from others, but I have had no personal experience with them. Those that I can describe from personal experience are entered separately as recipes of their own. And there are many, many other N-methyl homologues which have been prepared and characterized in the literature, and have yet to be tasted. So far, however, the only consistent thing seen is that, with N-methylation, the potency of the psychedelics is decreased, but the potency of the stimulants appears to be pretty much maintained."
  2. ^ 2.0 2.1 Shulgin A, Manning T, Daley P. The Shulgin Index, Volume One: Psychedelic Phenethylamines and Related Compounds 1. Berkeley: Transform Press. 2011: 344. ISBN 978-0-9630096-3-0. 
  3. ^ Clark C. The Identification of Methoxy-N-Methylamphetamines. Journal of Forensic Sciences. 1 October 1984, 29 (4): 1056–1071. ISSN 0022-1198. doi:10.1520/JFS11772J. 

外部链接

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