Exploring 2,6-DMA. To explore a different substance…

Names:
2,6-DMA · 2,6-Dimethoxyamphetamine
IUPAC name:
1-(2,6-Dimethoxyphenyl)propan-2-amine
ID: 2163 · Formula: C11H17NO2 · Molecular weight: 195.258
InChI: InChI=1S/C11H17NO2/c1-8(12)7-9-10(13-2)5-4-6-11(9)14-3/h4-6,8H,7,12H2,1-3H3

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. http://dx.doi.org/10.1002/omr.1270210611

Antun, F; Smythies, JR; Benington, F; Morin, RD; Barfknecht, CF; Nichols, DE. Native fluorescence and hallucinogenic potency of some amphetamines. Experientia, 15 Jan 1971, 27 (1), 62–63. 248 kB. http://dx.doi.org/10.1007/BF02137743

Domelsmith, LN; Eaton, TA; Houk, KN; Anderson, GM; Glennon, RA; Shulgin, AT; Castagnoli, N; Kollman, PA. Photoelectron spectra of psychotropic drugs. 6. Relationships between physical properties and pharmacological actions of amphetamine analogues. J. Med. Chem., 1 Jan 1981, 24 (12), 1414–1421. 963 kB. http://dx.doi.org/10.1021/jm00144a009

Glennon, RA; Liebowitz, SM; Anderson, GM. Serotonin receptor affinities of psychoactive phenalkylamine analogues. J. Med. Chem., 1 Mar 1980, 23 (3), 294–299. 844 kB. http://dx.doi.org/10.1021/jm00177a017

Shulgin, AT; Sargent, T; Naranjo, C. Structure-activity relationships of one-ring psychotomimetics. Nature, 1 Jan 1969, 221, 537–541. 537 kB. http://dx.doi.org/10.1038/221537a0

Bailey, K; Legauld, D; Verner, D. Spectroscopic and chromatographic identification of dimethoxyamphetamines. J. Assoc. Off. Anal. Chem., 1974, 57 (1), 70–78. 426 kB.

2,6-DNNA
N-Me-2,6-DMA
2,6-DMPEA
6-Br-2-MA
TMA-5
3,2,6-DOB · 3-Br-2,6-DMA
3-I-2,6-DMA
3-Me-2,6-DOM
3,2,6-DOET
ψ-DOM
TMA-6
2336
ψ-ALEPH
4,2,6-DOB · ψ-DOB
4,2,6-DOET · ψ-DOET
ψ-DOI
DOTFM-6
ψ-ALEPH-2
ψ-DODFE
ψ-MTFEM
ψ-MDFEM
ψ-MFEM
ψ-DOTFE
ψ-DODFMO
2-MA · 2-Methoxyamphetamine
1443
2,3-DMBZP · 2,6-DMBZP
2C-D
DESOXY
2,4-DMA
2,5-DMA
3,4-DMA
MEPEA
3,5-DMA
2,3-DMA
MM-GEA
N-Me-2,5-DMPEA · 25H-NMe
2,5-MH-MMA
2-DES-Me-DOM · 2-DM-DOM
5-DES-Me-DOM · 5-DM-DOM
4-Me-2,6-DMPEA · ψ-2C-D
2407
4-Ethoxynorephedrine
BO3MM
BO3ME
BO3MA
BO3E
N-Me-DMPEA-2
2,3-EMPEA
N-Me-DMPEA-3
2,4-EMPEA
Coryneine
N,N-Me-DHA
DHEA
MHMA
MH-α-Et-PEA
HMMA
β-Me-DMPEA
N-Me-DMPEA
EMPEA
β,2-HO-5,N-DMeA
β-HO-N-Me-2-M-5-MePEA
β-HO-2-M-5-MeA
N,N-Me-2,5-HMPEA
β-Me-2,5-DMPEA
N-Me-3,5-DMPEA
N-Me-2,6-DMPEA
6-Me-2,4-DMPEA
iso-2C-D
HMP
homo-3,4-DMPEA
N-MeO-PMA
2,6-DNNA
N-Me-2,6-DMA
2,6-DMPEA
6-Br-2-MA
TMA-5
3,2,6-DOB · 3-Br-2,6-DMA
3-I-2,6-DMA
3-Me-2,6-DOM
3,2,6-DOET
ψ-DOM
TMA-6
2336
ψ-ALEPH
4,2,6-DOB · ψ-DOB
4,2,6-DOET · ψ-DOET
ψ-DOI
DOTFM-6
ψ-ALEPH-2
ψ-DODFE
ψ-MTFEM
ψ-MDFEM
ψ-MFEM
ψ-DOTFE
ψ-DODFMO
2-MA · 2-Methoxyamphetamine
1443
2,3-DMBZP · 2,6-DMBZP
2C-D
DESOXY
2,4-DMA
2,5-DMA
3,4-DMA
MEPEA
3,5-DMA
2,3-DMA
MM-GEA
N-Me-2,5-DMPEA · 25H-NMe
2,5-MH-MMA
2-DES-Me-DOM · 2-DM-DOM
5-DES-Me-DOM · 5-DM-DOM
4-Me-2,6-DMPEA · ψ-2C-D
2407
4-Ethoxynorephedrine
BO3MM
BO3ME
BO3MA
BO3E
N-Me-DMPEA-2
2,3-EMPEA
N-Me-DMPEA-3
2,4-EMPEA
Coryneine
N,N-Me-DHA
DHEA
MHMA
MH-α-Et-PEA
HMMA
β-Me-DMPEA
N-Me-DMPEA
EMPEA
β,2-HO-5,N-DMeA
β-HO-N-Me-2-M-5-MePEA
β-HO-2-M-5-MeA
N,N-Me-2,5-HMPEA
β-Me-2,5-DMPEA
N-Me-3,5-DMPEA
N-Me-2,6-DMPEA
6-Me-2,4-DMPEA
iso-2C-D
HMP
homo-3,4-DMPEA
N-MeO-PMA
19 September 2017 · Creative Commons BY-NC-SA ·