Explore 3,4,5-Trimethoxybenzaldehyde | PiHKAL · info

Exploring 3,4,5-Trimethoxybenzaldehyde. To explore a different substance…

Name

3,4,5-TMBAL

IUPAC name

3,4,5-Trimethoxybenzaldehyde

ID 12330 · Formula C₁₀H₁₂O₄ · Molecular weight 196.2

InChI InChI=1S/C10H12O4/c1-12-8-4-7(6-11)5-9(13-2)10(8)14-3/h4-6H,1-3H3

InChI Key OPHQOIGEOHXOGX-UHFFFAOYSA-N This stereoisomer Any stereoisomer

SMILES COc1cc(C=O)cc(c1OC)OC

ChemSpider 6597
PubChem 6858
Wikidata Q15634093
Blotter 3,4,5-MeO-benzaldehyde
Rhodium 3,4,5-Trimethoxybenzaldehyde & syringaldehyde from 5-bromovanillin (V)
Rhodium MMDA & mescaline synthesis from vanillin
Rhodium Synthesis of mescaline from eucalyptus sawdust
Rhodium Mescaline chemistry monograph [from The Alkaloids, Vol. III]
Rhodium An improved synthesis of mescaline from gallic acid
Rhodium Alkylation of phenolic aldehydes with trimethyl phosphate
Rhodium 3,4,5-Trimethoxybenzaldehyde from p-Cresol (1)
Rhodium 3,4,5-Trimethoxybenzaldehyde from vanillin, 4-hydroxybenzaldehyde or p-cresol (1)
Rhodium 3,4,5-Trimethoxybenzaldehyde from gallic acid (3,4,5-trimethoxybenzoic acid)
Rhodium Synthesis of 3,4,5-trimethoxybenzaldehyde from vanillin

PiHKAL #1 AEM · #51 β-D · #96 M · #157 TMA

Cassels, BK; Sáez-Briones, P. DARK classics in chemical neuroscience: Mescaline. ACS Chem. Neurosci., 17 Oct 2018, 9 (10), 2448-2458. 648 kB. https://doi.org/10.1021/acschemneuro.8b00215

Chapman, SJ. Novel Psychoactive Spectra: NMR of (mostly) Novel Psychoactive Substances. BLOTTER, 25 Jun 2018, 3 (2). https://doi.org/10.16889/isomerdesign-6 #3,4,5-MeO-benzaldehyde NMR

Chambers, SA; DeSousa, JM; Huseman, ED; Townsend, SD. The DARK side of total synthesis: Strategies and tactics in psychoactive drug production. ACS Chem. Neurosci., 17 Oct 2018, 9 (10), 2307–2330. 8.1 MB. https://doi.org/10.1021/acschemneuro.7b00528 #213

Fenderson5555. Mescaline, part 1 of 3. , 14 Aug 2019. . Fenderson5555 8.4 MB. #3,4,5-TMBAL

Fenderson5555. Mescaline, part 3 of 3. , 17 Aug 2019. . Fenderson5555 11.9 MB. #3,4,5-TMBAL

Fenderson5555. Mescaline, part 2 of 3. , 17 Aug 2019. . Fenderson5555 13.6 MB. #3,4,5-TMBAL

Benington, F; Morin, RD; Clarke, LC. Synthesis of 4-hydroxy- and 4-ethoxy-3,5-dimethoxy-β-phenethylamines. J. Am. Chem. Soc., 1 Nov 1954, 76 (21), 5555–5556. 307 kB. https://doi.org/10.1021/ja01650a084 #3,4,5-Trimethoxybenzaldehyde

DMPAA · Homoveratric acid

2,3,6-TMBAL · 2,3,6-Trimethoxybenzaldehyde

2,4,5-TMBAL · 2,4,5-Trimethoxybenzaldehyde

2,4,6-TMBAL · 2,4,6-Trimethoxybenzaldehyde

2,3,4-TMBAL · 2,3,4-Trimethoxybenzaldehyde

2,3,5-TMBAL · 2,3,5-Trimethoxybenzaldehyde

4-EtO-3-HO-5-MBAL · 4-Ethoxy-3-hydroxy-5-methoxybenzaldehyde

Isosafrole glycol

3-EtO-5-HO-4-MBAL · 3-Ethoxy-5-hydroxy-4-methoxybenzaldehyde

7 Dec 2019 · · Isomer Design