Cannabis Ruderalis

MEE
Names
Preferred IUPAC name
1-(4,5-Diethoxy-2-methoxyphenyl)propan-2-amine
Other names
2-Methoxy-4,5-diethoxyphenethylamine
Identifiers
3D model (JSmol)
ChemSpider
UNII
  • 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
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 ?)

MEE (2-methoxy-4,5-diethoxyamphetamine) is a lesser-known psychedelic drug of the amphetamine class. It is a diethoxy-methoxy analog of TMA-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]


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