A crystallographic and theoretical study of the conformation of DOET and its significance for the hallucinogenic amphetamines
Journal of Pharmacy and Pharmacology 1975 Alan S. Horn, Michael L. Post, Olga Kennard et al. 4 citations
Abstract The crystal and molecular structure of 2,5-dimethoxy-4-ethyl-α-methyl-phenylethylamine (DOET) has been determined by X-ray crystallography and the conformation of the side chain has been examined theoretically by the use of a potential energy calculation. There is no indication in the solid state of any intra or inter-molecular hydrogen bonding. The isopropylamine side chain is...