EME (psychedelic)

EME

Names
Preferred IUPAC name

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

Identifiers

CAS Number

* 23693-34-7 Y

3D model (JSmol)

* Interactive image
* Interactive image

ChemSpider |

* 21106298 Y

PubChem CID

* 44719562

UNII |

* J5Z2GQ2QK7

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 Y

Key: IVHFHHXLFFHTTA-UHFFFAOYSA-N Y

* 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).

Y verify (what is YN ?)
Infobox references

Tracking categories (test):

* SizeSet

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.

## See also

* Phenethylamine
* Psychedelics, dissociatives and deliriants

## References

1. ↑ EME Entry in PiHKAL

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*[CID]: Compound ID