2,5-Dimethoxy-4-ethylamphetamine

2,5-Dimethoxy-4-ethylamphetamine
Clinical data
Other names	2,5-dimethoxy-4-ethylamphetamine
Legal status
Legal status	AU: S9 (Prohibited substance); BR: Class F2 (Prohibited psychotropics); CA: Schedule I; DE: Anlage I (Authorized scientific use only); UK: Class A; US: Schedule I; UN: Psychotropic Schedule I;
Identifiers
	IUPAC name 1-(4-Ethyl-2,5-dimethoxyphenyl)propan-2-amine;
CAS Number	22004-32-6 ;
PubChem CID	27402;
DrugBank	DB01467 ;
ChemSpider	25499 ;
UNII	9SK6K682UL;
KEGG	C22714 ;
ChEMBL	ChEMBL8224 ;
Chemical and physical data
Formula	C13H21NO2
Molar mass	223.316 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES O(c1cc(c(OC)cc1CC(N)C)CC)C;
	InChI InChI=1S/C13H21NO2/c1-5-10-7-13(16-4)11(6-9(2)14)8-12(10)15-3/h7-9H,5-6,14H2,1-4H3 ; Key:HXJKWPGVENNMCC-UHFFFAOYSA-N ;
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2,5-Dimethoxy-4-ethylamphetamine (DOET, DOE, Hecate) is a psychedelic drug of the phenethylamine and amphetamine chemical classes. It was first synthesized by Alexander Shulgin, and was described in his book PiHKAL (Phenethylamines i Have Known And Loved).

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