3-Me-2,4-DOM
 
1-(2,4-Dimethoxy-3-methylphenyl)propan-2-amine
 7006 ·  C12H19NO2 ·  209.285
 InChI=1S/C12H19NO2/c1-8(13)7-10-5-6-11(14-3)9(2)12(10)15-4/h5-6,8H,7,13H2,1-4H3
 XCEORCNVPWLEAY-UHFFFAOYSA-N This stereoisomer Any stereoisomer
 COc1c(ccc(c1C)OC)CC(N)C

Ho, B; McIsaac, WM; An, R; Tansey, LW; Walker, KE; Englert, LF; Noel, MB. Analogs of α-methylphenethylamine (amphetamine). I. Synthesis and pharmacological activity of some methoxy and/or methyl analogs. J. Med. Chem., 1 Jan 1970, 13 (1), 26–30. 601 kB. https://doi.org/10.1021/jm00295a007 #14

2C-E
2C-G
DOM
ψ-DOM
2,5-DMMA · METHYL-DMA
4C-DMA · 4C-H
4C-DMPEA
N-Me-2C-D
2C-D-2-EtO · 2CD-2ETO
2C-D-5-EtO · 2CD-5ETO
m-DOM · 5-DOM
o-DOM · 2-DOM
6-Me-2,4-DOM · Z-7.1
2,4-DMMA
ψ-2C-E
4-Propoxynorephedrine
homo-DMA
homo-N-Me-2,5-DMPEA
BO3MDM
BO3MEA
BO3EE
BO3P
N,N-Me-DMPEA-2
N-Me-2,3-DMA
N-Me-2,3-EMPEA
4C-2,4-DMPEA
2,4-DEPEA
N-Me,N-iPr-DHPEA
N-Bu-DHPEA
N-iBu-DHPEA
MHEA
N-Me-α-Et-GEA
Salicifoline
HMEA
N,N-Me-DMPEA
N-Et-DMPEA
DMMA
N-Me-EMPEA
EMA
MEA
DEPEA
β-HO-N-Me-2-M-5-MeA
N,N-Me-2,5-HMA
N,N-Me-2C-H
β,N-Me-2,5-DMPEA
N,N-Me-3,5-DMPEA
N-Me-3,5-DMA
N,N-Me-2,6-DMPEA
N-Me-2,6-DMA
4-Me-2,3-DOM
2-Me-3,4-DOM
5-Me-2,3-DOM
3-DOM
2-Me-3,5-DOM
BMD
5-Me-3,4-DOM
4-Me-3,5-DOM
6-Me-2,3-DOM
3-Me-2,6-DOM
2-Me-3,6-DOM
6-Me-2,4-EMPEA
2C-H-2-iPrO
10432
10408
DE
10096
10048
10034
10027
3,5-DMB
2C-H-5-iPrO
16 November 2018 · Creative Commons BY-NC-SA ·