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Names

DOHM
Hydroxy-DOM

IUPAC name

[4-(2-Aminopropyl)-2,5-dimethoxyphenyl]methanol

ID 1016 · Formula C₁₂H₁₉NO₃ · Molecular weight 225.284

InChI InChI=1S/C12H19NO3/c1-8(13)4-9-5-12(16-3)10(7-14)6-11(9)15-2/h5-6,8,14H,4,7,13H2,1-3H3

InChI Key PJNXHBSMCHLAFM-UHFFFAOYSA-N This stereoisomer Any stereoisomer

SMILES COc1cc(CO)c(cc1CC(N)C)OC

ChemSpider 62902104
PubChem 72440115

Shulgin Index See #60 DOM · Table 5Page 343Row 4

Phenethylamine: Von der Strucktur zur Funktion Hydroxy-DOM: 8.5 (202) 805, 812, 813

Ho, B; Tansey, LW. Analogs of amphetamine. 4. Synthesis of metabolites of 1-(2,5-dimethoxy-4-methylphenyl)-2-aminopropane (DOM). J. Med. Chem., 1 Feb 1971, 14 (2), 156–157. 316 kB. https://doi.org/10.1021/jm00284a018 #2

Ho, B; Estevez, V; Tansey, LW; Englert, LF; Creaven, PJ; McIsaac, WM. Analogs of amphetamine. 5. Excretory metabolites of 1-(2,5-dimethoxy-4-methylphenyl)-2-aminopropane (DOM) in rats. J. Med. Chem., 1 Feb 1971, 14 (2), 158–160. 371 kB. https://doi.org/10.1021/jm00284a019 #2 TLC,spot

BOD · β-Methoxy-2C-D

E · Escaline

ME

AMM · EA-1319 · TMA

2,4,5-TMA · TMA-2

TMA-3

TMA-4

TMA-5

TMA-6 · ψ-TMA-2

M-M · METHYL-MESCALINE

2C-O-2

N,N-Dimethyl-3-demethylmescaline · N,N-Me-3-DESMETHYL

N,N-Me-DME · Macromerine

2C-pEtOH

4C-HO

homo-Mescaline

Metiprenaline · β-HO-N-iPr-GEA

N-Me-β,3,4-TMPEA · β,3,4-Trimethoxy-N-methylphenethylamine

DMMAOH

DEE

β-HO-N,N-Me-2,5-DMPEA

β-HO-β,N-Me-2,5-DMPEA

β-HO-N-Me-2,5-DMA

β,2-HO-N-Me-5-EA

β-HO-2,5-DEPEA

β-HO-N,N-Me-3,5-DMPEA

N-HO-DOM

DESMETHYL-MM

2-Me-M

β-HO-DOM

N-MeO-3,4-DMA

ψ-2C-O-2

β-Methylmescaline

3-Me-2C-O

10411

6-Me-2C-O

α-Methoxy-2C-D

Terbutaline

2C-MOM

HOT-E

1760

4-MeO-DESOXY · 4-MeOMe-3,5-DMPEA

6937

7 Dec 2019 · · Isomer Design