Exploring 2C-TMA-5. To explore a different substance…

Names:
TMPEA-5
2C-TMA-5
2,3,6-Trimethoxyphenethylamine
IUPAC name:
2-(2,3,6-Trimethoxyphenyl)ethan-1-amine
307 · C11H17NO3 · 211.258
InChI=1S/C11H17NO3/c1-13-9-4-5-10(14-2)11(15-3)8(9)6-7-12/h4-5H,6-7,12H2,1-3H3
SOARXDWNNULVNL-UHFFFAOYSA-N This stereoisomer Any stereoisomer

Bailey, K; Legault, D. 13C NMR spectra and structure of mono-, di- and trimethoxyphenylethylamines and amphetamines. Org. Magn. Resonance, 1 Jun 1983, 21 (6), 391–396. 680 kB. https://doi.org/10.1002/omr.1270210611

Clark, LC; Benington, F; Morin, RD. The effects of ring-methoxyl groups on biological deamination of phenethylamines. J. Med. Chem., 1 May 1965, 8 (3), 353–355. 389 kB. https://doi.org/10.1021/jm00327a016

Matsuhiro, B; Furst, A. 2,3,6-Trimethoxynitrostyrene and its β-phenethylamine. J. Med. Chem., 1 Sep 1970, 13 (5), 973. 140 kB. https://doi.org/10.1021/jm00299a042

Brimblecombe, RW; Pinder, RM. Hallucinogenic agents, Wright-Scientechnica, Bristol, UK, 1 Jan 1975. 46.2 MB.

Merchant, J; Mountwala, A. Synthesis of some β-phenethylamine derivatives. I. J. Org. Chem., 1 Nov 1958, 23 (11), 1774-1776. 359 kB. https://doi.org/10.1021/jo01105a601 #XIV

BOHD
4-D
β-D
IM
M
TMPEA
TMPEA-6 · 2C-TMA-6
3,5-D
2,6-D
α-D
N-Me-3-DESMETHYL
DOOH
β-HO-2,5-DMA
β,3,4-HO-N-iPr-DHPEA · Isoprenaline
MHMAOH
N,N-Me-HME
N-Me-DME
β,3,4-TMPEA
DMAOH
β-HO-DMA
β-HO-4,3-EMPEA
β,2-HO-N-Me-5-MA
β-HO-N-Me-2,5-DMPEA
BODM
β-HO,Me-2,5-DMPEA
β,2-HO-N-Me-5-EPEA
β,2-HO-5-EA
β-HO-N-Me-3,5-DMPEA
β-HO-N-Me-2,6-DMPEA
TMPEA-4
N-HO-2C-D
α-Me-3-DESMETHYL
DESMETHYL-M
α-Me-DESMETHYL
10030
Orciprenaline
N-Methyl-3,4,5-trimethoxybenzylamine
α,β-D
10252
10066
19 June 2018 · Creative Commons BY-NC-SA ·