2C-O-4

2C-O-4
Names
	Preferred IUPAC name 2-{2,5-Dimethoxy-4-[(propan-2-yl)oxy]phenyl}ethan-1-amine
Identifiers
CAS Number	952006-65-4 ;
3D model (JSmol)	Interactive image;
ChemSpider	21106225 ;
PubChem CID	44719510;
UNII	1GFL65O0VB;
CompTox Dashboard (EPA)	DTXSID70894771 ;
	InChI InChI=1S/C13H21NO3/c1-9(2)17-13-8-11(15-3)10(5-6-14)7-12(13)16-4/h7-9H,5-6,14H2,1-4H3 Key: KAKXJLWAEMHHTL-UHFFFAOYSA-N ;
	SMILES CC(C)Oc1cc(OC)c(cc1OC)CCN;
Properties
Chemical formula	C13H21NO3
Molar mass	239.31 g/mol
	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

2C-O-4 (4-isopropoxy-2,5-dimethoxyphenethylamine) is a phenethylamine of the 2C family. It is also a positional isomer of isoproscaline and was probably first synthesized by Alexander Shulgin. It produces hallucinogenic, psychedelic, and entheogenic effects.^[1] Because of the low potency of 2C-O-4, and the inactivity of 2C-O, Shulgin felt that the 2C-O series would not be an exciting area for research, and did not pursue any further analogues.^[1]