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Contents

   



(Top)
 


1 See also  





2 References  














MEE (psychedelic)






تۆرکجه
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From Wikipedia, the free encyclopedia
 


MEE
Names
Preferred IUPAC name

1-(4,5-Diethoxy-2-methoxyphenyl)propan-2-amine

Other names

2-Methoxy-4,5-diethoxyphenethylamine

Identifiers

CAS Number

3D model (JSmol)

ChemSpider

PubChem CID

UNII

CompTox Dashboard (EPA)

  • InChI=1S/C14H23NO3/c1-5-17-13-8-11(7-10(3)15)12(16-4)9-14(13)18-6-2/h8-10H,5-7,15H2,1-4H3 checkY

    Key: LKJRFMXILZHUHU-UHFFFAOYSA-N checkY

  • InChI=1/C14H23NO3/c1-5-17-13-8-11(7-10(3)15)12(16-4)9-14(13)18-6-2/h8-10H,5-7,15H2,1-4H3

    Key: LKJRFMXILZHUHU-UHFFFAOYAA

  • CCOc1cc(OC)c(cc1OCC)CC(C)N

Properties

Chemical formula

C14H23NO3
Molar mass 253.342 g·mol−1

Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

checkY verify (what is checkY☒N ?)

Infobox references

MEE (2-methoxy-4,5-diethoxyamphetamine) is a lesser-known psychedelic drug of the amphetamine class. It is a diethoxy-methoxy analogofTMA-2. MEE was first synthesized by Alexander Shulgin. In his book PiHKAL, both the dosage and duration are unknown.[1] MEE produces few to no effects. Very little data exists about the pharmacological properties, metabolism, and toxicity of MEE.

See also[edit]

References[edit]


  • t
  • e

  • Retrieved from "https://en.wikipedia.org/w/index.php?title=MEE_(psychedelic)&oldid=1111849046"

    Categories: 
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    This page was last edited on 23 September 2022, at 07:25 (UTC).

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