2,6-DMPEA:
531,
537 ·
883
Bailey, K; Legault, D. 13C NMR spectra and structure of mono-, di- and trimethoxyphenylethylamines and amphetamines. Org. Magn. Resonance, 1 Jun 1983, 21 (6), 391–396. 680 kB. https://doi.org/10.1002/omr.1270210611 #2,6-DMPEA NMR
Clark, LC; Benington, F; Morin, RD. The effects of ring-methoxyl groups on biological deamination of phenethylamines. J. Med. Chem., 1 May 1965, 8 (3), 353–355. 389 kB. https://doi.org/10.1021/jm00327a016
Maher, HM; Awad, T; DeRuiter, J; Clark, CR. GC-MS and GC-IRD studies on dimethoxyphenethylamines (DMPEA): Regioisomers related to 2,5-DMPEA. J. Chromatogr. Sci., 1 Jan 2012, 50 (1), 1–9. 594 kB. https://doi.org/10.1093/chromsci/bmr013
Brimblecombe, RW; Pinder, RM. Hallucinogenic agents, Wright-Scientechnica, Bristol, UK, 1 Jan 1975. 46.2 MB. #Page 62
3,4-DMPEA · DMPEA · Homoveratrylamine
3-Methoxy-N-methyltyramine · N-Me-GEA
4-Methoxynorephedrine · β-HO-PMA
4-HO-3-MeO-A · 4-Hydroxy-3-methoxyamphetamine · HMA · MHA
β-O-Methylsynephrine · β-MeO-HMePEA
N,N-Dimethyldopamine · N,N-Me-DHPEA
3-Methoxy-2-trideuteromethoxyphenethylamine · IS