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Name

2C-D-2P

IUPAC name

1-(2,5-Dimethoxy-4-methylphenyl)propan-2-one

ID 7132 · Formula C₁₂H₁₆O₃ · Molecular weight 208.254

InChI InChI=1S/C12H16O3/c1-8-5-12(15-4)10(6-9(2)13)7-11(8)14-3/h5,7H,6H2,1-4H3

InChI Key HVGSPGNDKJUCDF-UHFFFAOYSA-N This stereoisomer Any stereoisomer

SMILES COc1cc(C)c(cc1CC(=O)C)OC

ChemSpider 518721
PubChem 596716
Wikidata Q82116281
Rhodium Azlactone route to phenyl-2-propanones from benzaldehydes (2C-D-2P)
Rhodium Synthesis of STP (DOM)

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 #4 TLC,spot

Coutts, RT; Malicky, JL. The synthesis of four possible in vitro metabolites of the hallucinogen 1-(2,5-dimethoxy-4-methylphenyl)-2-aminopropane (DOM) Can. J. Chem., 1 Feb 1974, 52 (3), 395–399. 299 kB. https://doi.org/10.1139/v74-063 #2b MS,NMR,IR

3,4,5-Trimethoxyphenylprop-2-ene · Elemicin

cis-3,4,5-Trimethoxyphenylprop-1-ene · cis-Isoelemicin

trans-3,4,5-Trimethoxyphenylprop-1-ene · Isoelemicin

2,4,5-Trimethoxyphenylprop-2-ene · γ-Asarone

cis-2,4,5-Trimethoxyphenylprop-1-ene · β-Asarone

trans-2,4,5-Trimethoxyphenylprop-1-ene · α-Asarone

4-Isopropropyl-2,5-dimethoxybenzaldehyde · 4-iPr-2,5-DMBAL

2C-E acetaldehyde

4-Me-2,5-DEBAL · 4-Methyl-2,5-diethoxybenzaldehyde

2-BuO-4-MBAL · 2-Butoxy-4-methoxybenzaldehyde

11138

11139

11140

11141

11142

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11144

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11149

4-Pr-2,5-DMBAL · 4-Propyl-2,5-dimethoxybenzaldehyde

7 Dec 2019 · · Isomer Design