EME (psychedelic)

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Find sources: "EME" psychedelic – news · newspapers · books · scholar · JSTOR (July 2019)

EME
Names

Preferred IUPAC name 1-(2,5-Diethoxy-4-methoxyphenyl)propan-2-amine
Identifiers
CAS Number	23693-34-7 ^checkY
3D model (JSmol)	Interactive image Interactive image
ChemSpider	21106298 ^checkY
PubChem CID	44719562
UNII	J5Z2GQ2QK7
CompTox Dashboard (EPA)	DTXSID80660363 Edit this at Wikidata
InChI InChI=1S/C14H23NO3/c1-5-17-12-9-13(16-4)14(18-6-2)8-11(12)7-10(3)15/h8-10H,5-7,15H2,1-4H3^checkY Key: IVHFHHXLFFHTTA-UHFFFAOYSA-N^checkY InChI=1/C14H23NO3/c1-5-17-12-9-13(16-4)14(18-6-2)8-11(12)7-10(3)15/h8-10H,5-7,15H2,1-4H3 Key: IVHFHHXLFFHTTA-UHFFFAOYAT
SMILES C1(=CC(=C(C=C1CC(C)N)OCC)OC)OCC COc1cc(OCC)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

Chemical compound

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

References

[edit ]

^ EME Entry in PiHKAL

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See also

References