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Names

4-HO-3-MeO-A
MHA

IUPAC name

4-(2-Aminopropyl)-2-methoxyphenol

ID 452 · Formula C₁₀H₁₅NO₂ · Molecular weight 181.232

InChI InChI=1S/C10H15NO2/c1-7(11)5-8-3-4-9(12)10(6-8)13-2/h3-4,6-7,12H,5,11H2,1-2H3

InChI Key GPBOYXOSSQEJBH-UHFFFAOYSA-N This stereoisomer Any stereoisomer

SMILES COc1cc(ccc1O)CC(N)C

ChemSpider 170725
PubChem 197139
Wikidata Q27291302
Project Response 1344-16

Shulgin Index #94 MHA · Table 4Page 329Row 12

Phenethylamine: Von der Strucktur zur Funktion MHA: 7.5 (28) 550, 572, 573

Fennoy, LV. Substituted phenylalanines and phenylethylamines. J. Org. Chem., 1 Nov 1961, 26 (11), 4696–4698. 279 kB. https://doi.org/10.1021/jo01069a516

Milhazes, N; Cunha-Oliveira, T; Martins, P; Garrido, J; Oliveira, C; Rego, AC; Borges, F. Synthesis and cytotoxic profile of 3,4-methylenedioxymethamphetamine (“Ecstasy”) and its metabolites on undifferentiated PC12 cells: A putative structure-toxicity relationship. Chem. Res. Toxicol., , 19 (10), 1294–2304. 204 kB. https://doi.org/10.1021/tx060123i #13 MS,NMR,other

2,5-DMPEA · 25H · 2C-H

3,4-DMPEA · DMPEA

N-Me-GEA

2,4-DMPEA · 24 · 24DMP

4-Methoxynorephedrine · β-HO-PMA

2,3-DMPEA

2,6-DMPEA

3,5-DMPEA

BO3M

β-HO-Hordenine

β-MeO-HMePEA

Oxilofrine · β-HO-HMA

β,4-DMPEA

N-HO-PMA · HOT-PMA

N,N-Me-2,3-DHPEA

β,2-MHPEA-3

2,4-HMA

N,N-Dimethyldopamine · N,N-Me-DHPEA

N-Et-DHPEA

3,4-HHMA · DHMA

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

HMA

5HMA

748

Etilefrine

m-Hydroxyephedrine

12414

AEME · Methylecgonidine

7 Dec 2019 · · Isomer Design