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

Names:
3,5-DMA · 3,5-Dimethoxyamphetamine
IUPAC name:
1-(3,5-Dimethoxyphenyl)propan-2-amine
ID: 2045 · Formula: C11H17NO2 · Molecular weight: 195.258
InChI: InChI=1S/C11H17NO2/c1-8(12)4-9-5-10(13-2)7-11(6-9)14-3/h5-8H,4,12H2,1-3H3

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

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

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

Ho, B; McIsaac, WM; An, R; Tansey, LW; Walker, KE; Englert, LF; Noel, MB. Analogs of α-methylphenethylamine (amphetamine). I. Synthesis and pharmacological activity of some methoxy and/or methyl analogs. J. Med. Chem., 1 Jan 1970, 13 (1), 26–30. 601 kB. http://dx.doi.org/10.1021/jm00295a007

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

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

3,5-DNNA
N-Me-3,5-DMA
3,5-DMPEA
4C-3,5-DMPEA
TMA-4
2,3,5-DOB · 2-Br-3,5-DMA
2-I-3,5-DMA
2-Me-3,5-DOM
2,3,5-DOET
4,3,5-DOB · 4-Br-3,5-DMA
3C-BZ
3C-E
TMA
3C-FBZ
3C-P
3C-IP
3C-B
3C-A
3C-S
3C-H
3C-AL
3C-CPM
3C-FEM
3C-DFE
3C-TFE
3C-FP
3C-IB
3C-MAL
2335
4-Me-3,5-DOM
4,3,5-DOET
α-Me-DESMETHYL
2321
2322
4,3,5-DOPR
3-MA · 3-Methoxyamphetamine
5-PhPr-2-MA
1024
1025
1026
2,4-Dimethoxycathinone
2,3-DMBZP · 3,5-DMBZP
2C-D
DESOXY
2,4-DMA
2,5-DMA
3,4-DMA
MEPEA
2,3-DMA
2,6-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
3,5-DNNA
N-Me-3,5-DMA
3,5-DMPEA
4C-3,5-DMPEA
TMA-4
2,3,5-DOB · 2-Br-3,5-DMA
2-I-3,5-DMA
2-Me-3,5-DOM
2,3,5-DOET
4,3,5-DOB · 4-Br-3,5-DMA
3C-BZ
3C-E
TMA
3C-FBZ
3C-P
3C-IP
3C-B
3C-A
3C-S
3C-H
3C-AL
3C-CPM
3C-FEM
3C-DFE
3C-TFE
3C-FP
3C-IB
3C-MAL
2335
4-Me-3,5-DOM
4,3,5-DOET
α-Me-DESMETHYL
2321
2322
4,3,5-DOPR
3-MA · 3-Methoxyamphetamine
5-PhPr-2-MA
1024
1025
1026
2,4-Dimethoxycathinone
2,3-DMBZP · 3,5-DMBZP
2C-D
DESOXY
2,4-DMA
2,5-DMA
3,4-DMA
MEPEA
2,3-DMA
2,6-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
11 December 2017 · Creative Commons BY-NC-SA ·