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Name

α-Carboxy-2C-D

IUPAC names

2-Amino-3-(2,5-dimethoxy-4-methylphenyl)propanoic acid
2,5-Dimethoxy-4-methylphenylalanine

ID 2374 · Formula C₁₂H₁₇NO₄ · Molecular weight 239.268

InChI InChI=1S/C12H17NO4/c1-7-4-11(17-3)8(6-10(7)16-2)5-9(13)12(14)15/h4,6,9H,5,13H2,1-3H3,(H,14,15)

InChI Key MWCDQZBPLTYYSP-UHFFFAOYSA-N This stereoisomer Any stereoisomer

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

ChemSpider 2283749
PubChem 3015652
Wikidata Q82934207

Coutts, RT; Malicky, JL. The synthesis of some analogs of the hallucinogen 1-(2,5-dimethoxy-4-methylphenyl)-2-aminopropane (DOM). III. Some derivatives of 3-phenylalanine. Can. J. Chem., 1 Feb 1974, 52 (3), 390–394. 316 kB. https://doi.org/10.1139/v74-062 #2a NMR,IR

Ho, B; Tansey, LW; Huang, J. Analogs of amphetamine. 6. 2,5-Dimethoxy-4-methyl- and 2,5-dimethoxy-α,4-dimethylphenylalanines. J. Med. Chem., 1 Nov 1971, 14 (11), 1132–1133. 349 kB. https://doi.org/10.1021/jm00293a036 #1

Nichols, DE. Structure-activity relationships of phenethylamine hallucinogens. J. Pharm. Sci., 1 Aug 1981, 70 (8), 839–849. 1.4 MB. https://doi.org/10.1002/jps.2600700802 #XXVIIIa

DMMDA

DMMDA-2

N-Acetyl-3-demethymescaline

N-Formylmescaline

DOCA

N-Formyl-β-hydroxy-3,4-dimethoxy-N-methylphenethylamine · N-Me,CHO-DME

N-Me-2C-DMMDA-3

DMMDA-3

N-Me-2C-DMMDA

N-Me-2C-DMMDA-2

DMMDA-5

DMMDA-4

DMMDA-6

Methyldopate

11184

N-methyl-β-oxomescaline · β-Keto-N-methylmescaline · βk-M-M

7 Dec 2019 · · Isomer Design