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Name

2,5-DMBAL

IUPAC name

2,5-Dimethoxybenzaldehyde

ID 12313 · Formula C₉H₁₀O₃ · Molecular weight 166.174

InChI InChI=1S/C9H10O3/c1-11-8-3-4-9(12-2)7(5-8)6-10/h3-6H,1-2H3

InChI Key AFUKNJHPZAVHGQ-UHFFFAOYSA-N This stereoisomer Any stereoisomer

SMILES COc1ccc(c(c1)C=O)OC

ChemSpider 60092
PubChem 66726
Wikidata Q4596796
Blotter 2,5-MeO-benzaldehyde
Rhodium Synthesis of 2C-B from anise oil
Rhodium Synthesis of 2,5-dimethoxybenzaldehyde

PiHKAL #8 ARIADNE · #20 2C-B · #32 2C-H · #38 2C-SE · #54 2,5-DMA · #138 MPM

DeRuiter, J; Clark, R; Noggle, FT. LC and GC—MS analysis of 4-bromo-2,5-dimethoxyphenethylamine (Nexus) and 2-propanamine and 2-butanamine analogues. J. Chromatogr. Sci., 1 Oct 1995, 33 (10), 583–590. 1.2 MB. https://doi.org/10.1093/chromsci/33.10.583 #2,5-Dimethoxybenzaldehyde GC,LC,MS

Chapman, SJ. Novel Psychoactive Spectra: NMR of (mostly) Novel Psychoactive Substances. BLOTTER, 25 Jun 2018, 3 (2). https://doi.org/10.16889/isomerdesign-6 #2,5-MeO-benzaldehyde NMR

Ehlers, D; Schäning, J. Synthese von DOC (2,5-dimethoxy-4-chloramphetamin). Toxichem Krimtech, 1 Jan 2001, 68 (2), 62–68. 185 kB. #1 MS,NMR,IR,UV

Waumans, D; Bruneel, N; Tytgat, J. Anise oil as a precursor for 2-alkoxy-5-methoxybenzaldehydes. Microgram J., 1 Jan 2004, 2 (1–4), 4–10. 114 kB. #5 MS,NMR

Poulie, CBM; Jensen, AA; Halberstadt, AL; Kristensen, JL. DARK Classics in Chemical Neuroscience: NBOMes. ACS Chem. Neurosci., 12 Nov 2019, n/a. 338 kB. https://doi.org/10.1021/acschemneuro.9b00528 #1

Cheng, AC; Castagnoli, N. Synthesis and physicochemical and neurotoxicity studies of 1-(4-substituted-2,5-dihydroxyphenyl)-2-aminoethane analogs of 6-hydroxydopamine. J. Med. Chem., 1 Apr 1984, 27 (4), 513–520. 1.2 MB. https://doi.org/10.1021/jm00370a014 #6a

3,4-Dihydroxyphenylacetone · DHPA

3,5-DMBAL

2,3-DMBAL

2,4-DMBAL

2,6-DMBAL

3,4-DMBAL · Veratraldehyde

5-HO-4-Me-2-MBAL

11101

7 Dec 2019 · · Isomer Design