EME (psychedelic)

EME
Names
	Preferred IUPAC name 1-(2,5-Diethoxy-4-methoxyphenyl)propan-2-amine
Identifiers
CAS Number	23693-34-7 ;
3D model (JSmol)	Interactive image; Interactive image;
ChemSpider	21106298 ;
PubChem CID	44719562;
UNII	J5Z2GQ2QK7;
CompTox Dashboard (EPA)	DTXSID80660363 ;
	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 Key: IVHFHHXLFFHTTA-UHFFFAOYSA-N ; 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). verify (what is ?) Infobox references

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

^ EME Entry in PiHKAL

This psychoactive drug-related article is a stub. You can help Wikipedia by expanding it.

[1] EME Entry in PiHKAL

[1]

See also

References