Exploring 2,6-DMPEA. To explore a different substance…

Name:
2,6-DMPEA
IUPAC name:
2-(2,6-Dimethoxyphenyl)ethan-1-amine
ID: 449 · Formula: C10H15NO2 · Molecular weight: 181.232
InChI: InChI=1S/C10H15NO2/c1-12-9-4-3-5-10(13-2)8(9)6-7-11/h3-5H,6-7,11H2,1-2H3
InChI Key: VIHNHLSXVPNVPY-UHFFFAOYSA-NThis stereoisomerAny stereoisomer

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

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.

2C-H
3,4-DMPEA · DMPEA
N-Me-GEA
2,4-DMPEA
β-HO-PMA · 4-Methoxynorephedrine
2,3-DMPEA
3,5-DMPEA
MHA
BO3M
β-HO-Hordenine
β-MeO-HMePEA
β-HO-HMA · Oxilofrine
β,4-DMPEA
N-HO-PMA
N,N-Me-2,3-DHPEA
β,2-MHPEA-3
2,4-HMA
N,N-Me-DHPEA
N-Et-DHPEA
3,4-HHMA
DH-α-Et-PEA
β-Me-GEA
N-Me-HMPEA
HMA
β,2-HO-5,N-MePEA
β,2-HO-5-MeA
β-HO-2-M-5-MePEA
2,5-HMA
2,5-DES-Me-DOM
597
5HMA
HMA
m-Hydroxyephedrine
Etilefrine
748
12414
24 May 2018 · Creative Commons BY-NC-SA ·